Canonical Allele Identifier: PA331453
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90880
ClinVar RCV Id: RCV000076382 RCV001355702 RCV002415563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly692Val
CA019969
NM_000251.3:c.2075G>T