Canonical Allele Identifier: PA2580430264
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076457
ClinVar RCV Id: RCV002972326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Thr285Met
CA414005199
NM_020766.3:c.854C>T