Canonical Allele Identifier: PA2828047649
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13917
ClinVar RCV Id: RCV000014937 RCV000014938 RCV000163338 RCV000082051 RCV000420446 RCV000430685 RCV000431794 RCV000420995 RCV000552504 RCV000677899 RCV003460479
ClinVar Variation Id: 2779200
ClinVar RCV Id: RCV003645988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Cys380Arg
CA008315
NM_001355216.1:c.1138T>C
CA2739265341
NM_001355216.1:c.1137_1138delinsTC