Allele Registry

Canonical Allele Identifier: PA2828721432

Gene: GPHN HGNC NCBI

ClinVar Allele:

94254

ClinVar RCV:

RCV000074361

ClinVar Variation:

88674

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364445.1:p.Asp620Ala	CA145288 NM_001377516.1:c.1859A>C