Canonical Allele Identifier: PA645381751
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly749Arg
CA10578101
NM_000179.3:c.2245G>A
CA346752630
NM_000179.3:c.2245G>C