Canonical Allele Identifier: PA2825088011
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys428Thr
CA346744138
NM_000179.3:c.1283A>C