Canonical Allele Identifier: PA913193395
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 630106
ClinVar RCV Id: RCV001051464 RCV000775112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala609Gly
CA346728366
NM_000251.3:c.1826C>G