Canonical Allele Identifier: PA2826134974
Gene: STX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171511.1:p.Glu70Asp
CA6020768
NM_001178040.1:c.210G>C
CA380795702
NM_001178040.1:c.210G>T