Canonical Allele Identifier: PA916055211
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 665292
ClinVar RCV Id: RCV000823545 RCV002434025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ala866Thr
CA376556801
NM_020975.6:c.2596G>A