Canonical Allele Identifier: PA2826148645
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716381
ClinVar RCV Id: RCV002303449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Ser263Arg
CA414008114
NM_001184880.2:c.789C>G
CA414008116
NM_001184880.2:c.789C>A
CA414008131
NM_001184880.2:c.787A>C