Canonical Allele Identifier: PA2826637769
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129084
ClinVar RCV Id: RCV003057901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu932Asp
CA346760982
NM_001281494.2:c.2796A>C
CA346760983
NM_001281494.2:c.2796A>T