Canonical Allele Identifier: PA2826629239
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1187Asp
CA072360
NM_001281492.2:c.3559C>G