Canonical Allele Identifier: PA2828048596
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1483934
ClinVar RCV Id: RCV002003308 RCV002258350 RCV003464359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Leu621Val
CA376557018
NM_001355216.1:c.1861T>G