Canonical Allele Identifier: PA2825553293
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1523855
ClinVar RCV Id: RCV002039196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Glu249Asp
CA414008344
NM_001105243.2:c.747A>T
CA414008346
NM_001105243.2:c.747A>C