Canonical Allele Identifier: PA299483
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1173Met
CA013259
NM_000179.3:c.3517G>A