Canonical Allele Identifier: PA916011558
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys9Asn
CA016664
NM_001281494.2:c.27A>T
CA346740759
NM_001281494.2:c.27A>C