Canonical Allele Identifier: PA658804080
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525696
ClinVar RCV Id: RCV000629899 RCV004002780 RCV002420671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala710Gly
CA034290
NM_000251.3:c.2129C>G