Canonical Allele Identifier: PA2825553316
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 692247
ClinVar RCV Id: RCV000853589
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Asp266Glu
CA414008061
NM_001105243.2:c.798C>A
CA414008063
NM_001105243.2:c.798C>G