Canonical Allele Identifier: PA177589
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 164914
ClinVar RCV Id: RCV000151628 RCV000343106 RCV000890106 RCV000988360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149045.3:p.Arg962Cys
CA177588
NM_033056.4:c.2884C>T