Canonical Allele Identifier: PA2826148618
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 848462
ClinVar RCV Id: RCV001052229
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Asn234Asp
CA414008587
NM_001184880.2:c.700A>G