Canonical Allele Identifier: PA177606
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 164929
ClinVar RCV Id: RCV000151637 RCV001835689 RCV002516047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149045.3:p.Leu381Val
CA177605
NM_033056.4:c.1141C>G