Canonical Allele Identifier: PA1139690268
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842691
ClinVar RCV Id: RCV001045149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn5Asp
CA346740736
NM_001281494.2:c.13A>G