Canonical Allele Identifier: PA2826465515
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479800
ClinVar Variation Id: 659154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile728Leu
CA346730098
NM_001258281.1:c.2182A>T
CA346730100
NM_001258281.1:c.2182A>C