Canonical Allele Identifier: PA2829954180
Gene: PCDH19 HGNC NCBI

Linked Data

ClinVar Variation Id: 947224
ClinVar RCV Id: RCV001218248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065817.2:p.Glu870Asp
CA414000044
NM_020766.3:c.2610G>C
CA414000045
NM_020766.3:c.2610G>T