Canonical Allele Identifier: PA2741999669
Gene: STX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2580528
ClinVar RCV Id: RCV003329723
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443106.1:p.Glu233Asp
CA280568546
NM_052874.4:c.699G>C
CA395646911
NM_052874.4:c.699G>T