Canonical Allele Identifier: PA2826465661
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn769Asp
CA020655
NM_001258281.1:c.2305A>G