Canonical Allele Identifier: PA2573165097
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490228
ClinVar RCV Id: RCV002001702 RCV003471238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His639Pro
CA346728653
NM_000251.3:c.1916A>C