Canonical Allele Identifier: PA2826464005
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455481
ClinVar RCV Id: RCV000547106 RCV000774563 RCV004003729
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys357Glu
CA027338
NM_001258281.1:c.1069A>G