Canonical Allele Identifier: PA2580430251
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716381
ClinVar RCV Id: RCV002303449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Ser263Arg
CA414008114
NM_020766.3:c.789C>G
CA414008116
NM_020766.3:c.789C>A
CA414008131
NM_020766.3:c.787A>C