Canonical Allele Identifier: PA2828721024
Gene: GPHN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364444.1:p.Asp623Ala
CA145288
NM_001377515.1:c.1868A>C