Canonical Allele Identifier: PA2826634693
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe159Ser
CA346745004
NM_001281494.2:c.476T>C