Canonical Allele Identifier: PA2828721840
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 88674
ClinVar RCV Id: RCV000074361
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364446.1:p.Asp604Ala
CA145288
NM_001377517.1:c.1811A>C