Canonical Allele Identifier: PA2573061945
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1329378
ClinVar RCV Id: RCV001799421
ClinVar Variation Id: 1779882
ClinVar RCV Id: RCV002403991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met592Ile
CA346728280
NM_000251.3:c.1776G>A
CA346728281
NM_000251.3:c.1776G>C
CA346728282
NM_000251.3:c.1776G>T