Canonical Allele Identifier: PA2826465669
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 684444
ClinVar RCV Id: RCV000844898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro771Arg
CA346730714
NM_001258281.1:c.2312C>G