Canonical Allele Identifier: PA334597
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188316
ClinVar RCV Id: RCV000168313 RCV000213407 RCV000589584 RCV000735967 RCV001580463 RCV003462262 RCV003995623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His785Arg
CA020496
NM_000251.3:c.2354A>G