Canonical Allele Identifier: PA2826637666
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732522
ClinVar RCV Id: RCV002337617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg880Ile
CA346760255
NM_001281494.2:c.2639G>T