Canonical Allele Identifier: PA2825089187
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785679
ClinVar RCV Id: RCV002423991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile696Met
CA346750848
NM_000179.3:c.2088T>G