Canonical Allele Identifier: PA106594
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13944
ClinVar RCV Id: RCV000014971 RCV000414355 RCV000736274 RCV001013275 RCV001851862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys609Arg
CA007804
NM_020975.6:c.1825T>C