Canonical Allele Identifier: PA658807899
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 504714
ClinVar RCV Id: RCV000614177 RCV000965805 RCV004530735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136241.1:p.Glu1649Asp
CA5504768
NM_001142769.3:c.4947A>C
CA376520014
NM_001142769.3:c.4947A>T