Canonical Allele Identifier: PA128239
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24913
ClinVar RCV Id: RCV000519407 RCV000696792 RCV000564566 RCV001818172 RCV003460488 RCV002477000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Asp631Asn
CA008190
NM_020630.6:c.1891G>A