Canonical Allele Identifier: PA2826148669
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Arg284His
CA333826084
NM_001184880.2:c.851G>A