Canonical Allele Identifier: PA2573280679
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395976
ClinVar RCV Id: RCV001887315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Ser454Asn
CA2573159041
NM_020766.3:c.1360_1361delinsAA