Canonical Allele Identifier: PA2827855429
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1120072
ClinVar RCV Id: RCV001449716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341358.1:p.Glu1193Asp
CA376518047
NM_001354429.2:c.3579A>T
CA376518048
NM_001354429.2:c.3579A>C