Canonical Allele Identifier: PA645474168
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237358
ClinVar RCV Id: RCV000229489 RCV000479748 RCV000662583 RCV001017396 RCV001193852 RCV003491996 RCV003998751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln377Arg
CA027052
NM_000251.3:c.1130A>G