Canonical Allele Identifier: PA2826636535
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2834716
ClinVar RCV Id: RCV003758334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile589Val
CA069415
NM_001281494.2:c.1765A>G