Canonical Allele Identifier: PA2741966776
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2552405
ClinVar RCV Id: RCV003287748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Gly409Ala
CA10468907
NM_020766.3:c.1226G>C