Canonical Allele Identifier: PA2829954176
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2129183
ClinVar RCV Id: RCV003057950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Glu862Asp
CA414000142
NM_020766.3:c.2586G>T
CA414000143
NM_020766.3:c.2586G>C