Canonical Allele Identifier: PA190092
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr327Ser
CA016745
NM_000179.3:c.980C>G
CA346741015
NM_000179.3:c.979A>T