Canonical Allele Identifier: PA645479525
Gene: STX16 HGNC NCBI

Linked Data

ClinVar Variation Id: 339049
ClinVar RCV Id: RCV000280288 RCV000499786 RCV000893064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001433.1:p.Glu152Asp
CA9925324
NM_001001433.3:c.456G>T
CA409445000
NM_001001433.3:c.456G>C