Canonical Allele Identifier: PA2825553263
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754507
ClinVar RCV Id: RCV003098310 RCV002375882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098713.1:p.Thr221Ser
CA10468963
NM_001105243.2:c.661A>T
CA414008790
NM_001105243.2:c.662C>G