Canonical Allele Identifier: PA658832872
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 560653
ClinVar RCV Id: RCV000678824
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asp305Gly
CA414005027
NM_001184880.2:c.914A>G