Canonical Allele Identifier: PA2826148674
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2730973
ClinVar RCV Id: RCV003511372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171809.1:p.Gln290His
CA10468941
NM_001184880.2:c.870G>T
CA414005117
NM_001184880.2:c.870G>C