Canonical Allele Identifier: PA2826463279
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479794
ClinVar RCV Id: RCV000562138 RCV001222036 RCV004000851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser189Arg
CA346732397
NM_001258281.1:c.565A>C
CA346732404
NM_001258281.1:c.567T>A
CA346732405
NM_001258281.1:c.567T>G