Canonical Allele Identifier: PA2828048617
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1471458
ClinVar RCV Id: RCV001966786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Val628Ile
CA376557131
NM_001355216.1:c.1882G>A