Canonical Allele Identifier: PA2829939315
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 405541
ClinVar RCV Id: RCV000463969 RCV001015286 RCV001104288 RCV001105645 RCV001105646 RCV001105647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg79Trp
CA038673
NM_020630.6:c.235C>T