Canonical Allele Identifier: PA915980135
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 18429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136241.1:p.Val540Asp
CA253349
NM_001142769.3:c.1619T>A