Canonical Allele Identifier: PA2826636116
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg489Cys
CA010130
NM_001281494.2:c.1465C>T