Canonical Allele Identifier: PA2825827187
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 990887
ClinVar RCV Id: RCV001279000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136239.1:p.Thr563Ser
CA376515304
NM_001142767.2:c.1688C>G
CA376515310
NM_001142767.2:c.1687A>T