Canonical Allele Identifier: PA2573176083
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 1358516
ClinVar RCV Id: RCV001878650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Thr1020Ile
CA345941650
NM_001006657.2:c.3059C>T