Canonical Allele Identifier: PA2826624839
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1388690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val101Leu
CA346739933
NM_001281492.2:c.301G>C
CA346739938
NM_001281492.2:c.301G>T