Canonical Allele Identifier: PA230691
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 126976
ClinVar RCV Id: RCV000114837 RCV000115546 RCV000699802 RCV001800400 RCV003997208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr292Ser
CA022468
NM_000251.3:c.874A>T
CA346732887
NM_000251.3:c.875C>G