Canonical Allele Identifier: PA2826465444
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408475
ClinVar RCV Id: RCV000468999 RCV000492021 RCV001270006 RCV003168800 RCV003463906 RCV004000779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile708Val
CA16610892
NM_001258281.1:c.2122A>G