Canonical Allele Identifier: PA2826462825
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91044
ClinVar RCV Id: RCV000076546 RCV002433581 RCV002465507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu27Phe
CA020925
NM_001258281.1:c.79C>T