Canonical Allele Identifier: PA2826148863
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747094
ClinVar RCV Id: RCV003509355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Lys527Asn
CA414002410
NM_001184880.2:c.1581G>T
CA414002411
NM_001184880.2:c.1581G>C