Canonical Allele Identifier: PA2826465813
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182587
ClinVar RCV Id: RCV000203841 RCV000565478 RCV000708846 RCV000759828 RCV001354344 RCV001193897 RCV003467250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala803Glu
CA020801
NM_001258281.1:c.2408C>A