Canonical Allele Identifier: PA2829941305
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299894
ClinVar RCV Id: RCV000263988 RCV000260802 RCV000305137 RCV000359923 RCV000573672 RCV000697839 RCV001252827 RCV003153554 RCV002480091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg540Gly
CA034653
NM_020630.6:c.1618A>G