Allele Registry

Canonical Allele Identifier: PA2828721568

Gene: GPHN HGNC NCBI

ClinVar RCV:

RCV000642138

ClinVar Variation:

534546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364446.1:p.Val103Ile	CA7233727 NM_001377517.1:c.307G>A