Canonical Allele Identifier: PA658676629
Gene: CDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 452290
ClinVar RCV Id: RCV000520436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004924.1:p.Leu528Phe
CA397140963
NM_004933.3:c.1582C>T