Canonical Allele Identifier: PA2826634309
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr25Pro
CA346741012
NM_001281494.2:c.73A>C