Canonical Allele Identifier: PA2826635149
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe267Leu
CA346748540
NM_001281494.2:c.799T>C
CA346748550
NM_001281494.2:c.801C>A
CA346748554
NM_001281494.2:c.801C>G