Canonical Allele Identifier: PA215904
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41843
ClinVar RCV Id: RCV000034775 RCV000411986 RCV000458385 RCV000409131 RCV000568654 RCV001104859 RCV001104860 RCV001104857 RCV001104858 RCV002477061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Lys994Asn
CA009156
NM_020630.6:c.2982A>C
CA376558122
NM_020630.6:c.2982A>T