Canonical Allele Identifier: PA645391350
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 282913
ClinVar RCV Id: RCV000358392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136241.1:p.Ser1714Arg
CA10604342
NM_001142769.3:c.5142T>A
CA376518899
NM_001142769.3:c.5142T>G
CA376518912
NM_001142769.3:c.5140A>C