Canonical Allele Identifier: PA2826465157
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785840
ClinVar RCV Id: RCV002424152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala634Gly
CA346729232
NM_001258281.1:c.1901C>G