Canonical Allele Identifier: PA916004777
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339049
ClinVar RCV Id: RCV000280288 RCV000499786 RCV000893064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191797.1:p.Glu99Asp
CA9925324
NM_001204868.2:c.297G>T
CA409445000
NM_001204868.2:c.297G>C