Canonical Allele Identifier: PA2826630743
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe294Ile
CA009191
NM_001281493.2:c.880T>A