Canonical Allele Identifier: PA2826634329
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768750
ClinVar RCV Id: RCV002382967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu30Asp
CA346741137
NM_001281494.2:c.90A>T
CA346741142
NM_001281494.2:c.90A>C