Canonical Allele Identifier: PA645475822
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408486
ClinVar RCV Id: RCV002230804 RCV001015446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala804Thr
CA16610824
NM_000251.3:c.2410G>A