Allele Registry

Canonical Allele Identifier: PA2580119302

Gene: STX19 HGNC NCBI

ClinVar RCV:

RCV004164351

ClinVar Variation:

2319991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001850.1:p.Val79Met	CA353677330 NM_001001850.3:c.235G>A