Canonical Allele Identifier: PA177602
Gene: PCDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 164927
ClinVar RCV Id: RCV000151635 RCV001071653 RCV001103156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149045.3:p.Asn419Ser
CA177601
NM_033056.4:c.1256A>G