Allele Registry

Canonical Allele Identifier: PA658820247

Gene: GPHN HGNC NCBI

ClinVar RCV:

RCV000642138

ClinVar Variation:

534546

HGVS (amino-acid)	Matching Registered Transcripts
NP_065857.1:p.Val103Ile	CA7233727 NM_020806.5:c.307G>A