Canonical Allele Identifier: PA2829955545
Gene: WDR35 HGNC NCBI
ClinVar RCV:
RCV000000038
ClinVar Variation:
21
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Glu615Gly
CA339780
NM_020779.4:c.1844A>G