Canonical Allele Identifier: PA133439
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 44036
ClinVar RCV Id: RCV000037011 RCV000965135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136241.1:p.Gly1746Ser
CA133438
NM_001142769.3:c.5236G>A