Allele Registry

Canonical Allele Identifier: PA2828721528

Gene: GPHN HGNC NCBI

ClinVar RCV:

RCV000642141

RCV003338709

ClinVar Variation:

534549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364446.1:p.Asn29Ser	CA7233631 NM_001377517.1:c.86A>G