Canonical Allele Identifier: PA2826637493
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 486896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn809His
CA346758718
NM_001281494.2:c.2425A>C