Canonical Allele Identifier: PA2741966836
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2505843
ClinVar RCV Id: RCV003236075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Asp481Asn
CA414002722
NM_020766.3:c.1441G>A