Canonical Allele Identifier: PA331237
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90560
ClinVar RCV Id: RCV000236371 RCV000491838 RCV000627704 RCV000781559 RCV001030704 RCV003466962 RCV003997143 RCV004528275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly40Ser
CA017443
NM_000251.3:c.118G>A