Canonical Allele Identifier: PA2826631096
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys374Arg
CA009570
NM_001281493.2:c.1121A>G