Canonical Allele Identifier: PA2826148607
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754507
ClinVar RCV Id: RCV003098310 RCV002375882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Thr221Ser
CA10468963
NM_001184880.2:c.661A>T
CA414008790
NM_001184880.2:c.662C>G