Canonical Allele Identifier: PA2826148680
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 947804
ClinVar RCV Id: RCV001218941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Gly296Val
CA414005077
NM_001184880.2:c.887G>T