Canonical Allele Identifier: PA2826463445
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230546
ClinVar RCV Id: RCV000220130 RCV000411007 RCV000469366 RCV000589679 RCV003997848
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp229Glu
CA041012
NM_001258281.1:c.687C>G
CA346732909
NM_001258281.1:c.687C>A