Canonical Allele Identifier: PA138391
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 46453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149045.3:p.Arg855Trp
CA138390
NM_033056.4:c.2563C>T