Canonical Allele Identifier: PA2826465161
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044545
ClinVar RCV Id: RCV002903769 RCV003585314
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu635Gly
CA46702673
NM_001258281.1:c.1904A>G