Canonical Allele Identifier: PA2826634786
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772977
ClinVar RCV Id: RCV002394633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu182Asp
CA346745706
NM_001281494.2:c.546A>C
CA346745710
NM_001281494.2:c.546A>T