Canonical Allele Identifier: PA2826462936
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91119
ClinVar RCV Id: RCV000570883 RCV000627693 RCV001137124 RCV003231115 RCV003997176
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg105Lys
CA021254
NM_001258281.1:c.314G>A