Canonical Allele Identifier: PA2826634296
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys22Asn
CA10578055
NM_001281494.2:c.66A>C
CA346740965
NM_001281494.2:c.66A>T