Canonical Allele Identifier: PA658671069
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 466213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065857.1:p.Asn267Ser
CA7233831
NM_020806.5:c.800A>G