Canonical Allele Identifier: PA2826629549
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110673
ClinVar RCV Id: RCV003020300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg14Met
CA346740805
NM_001281493.2:c.41G>T