Canonical Allele Identifier: PA2826463440
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479808
ClinVar RCV Id: RCV000562750
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe228Cys
CA346732899
NM_001258281.1:c.683T>G