Canonical Allele Identifier: PA2826465415
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483660
ClinVar RCV Id: RCV000561684 RCV000698314 RCV000758591 RCV001764664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala699Val
CA346729845
NM_001258281.1:c.2096C>T