Canonical Allele Identifier: PA2826631398
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly447Arg
CA10578101
NM_001281493.2:c.1339G>A
CA346752630
NM_001281493.2:c.1339G>C