Canonical Allele Identifier: PA645471156
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422056
ClinVar RCV Id: RCV000484092 RCV000564344 RCV000811394 RCV001358224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr43Phe
CA16617550
NM_000251.3:c.128A>T