Canonical Allele Identifier: PA2828047698
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241342
ClinVar RCV Id: RCV000229577 RCV000662388 RCV001292757 RCV002508206 RCV002411060 RCV003463677 RCV002487084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ala387Thr
CA036607
NM_001355216.1:c.1159G>A