Canonical Allele Identifier: PA2826637673
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587318
ClinVar RCV Id: RCV003360799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly884Ser
CA346760278
NM_001281494.2:c.2650G>A