Canonical Allele Identifier: PA2826633395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 934973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His901Arg
CA346760564
NM_001281493.2:c.2702A>G