Canonical Allele Identifier: PA112747
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV000000038
ClinVar Variation:
21
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006658.1:p.Glu626Gly
CA339780
NM_001006657.2:c.1877A>G