Canonical Allele Identifier: PA2825553087
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 578043
ClinVar RCV Id: RCV000700933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Glu31Lys
CA414011397
NM_001105243.2:c.91G>A