Canonical Allele Identifier: PA916012286
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn971Lys
CA072193
NM_001281494.2:c.2913T>G
CA346761246
NM_001281494.2:c.2913T>A