Canonical Allele Identifier: PA2826464788
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489924
ClinVar RCV Id: RCV000580277 RCV001063386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala549Val
CA031700
NM_001258281.1:c.1646C>T