Canonical Allele Identifier: PA916011151
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn93Asp
CA073334
NM_001281492.2:c.277A>G