Allele Registry

Canonical Allele Identifier: PA2828721155

Gene: GPHN HGNC NCBI

ClinVar RCV:

RCV000548955

RCV002526142

ClinVar Variation:

466209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364445.1:p.Ala91Thr	CA7233704 NM_001377516.1:c.271G>A