Canonical Allele Identifier: PA2830277991
Gene: WDR36 HGNC NCBI

Linked Data

ClinVar Variation Id: 350330
ClinVar RCV Id: RCV000961645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_644810.2:p.Met615Val
CA3365888
NM_139281.3:c.1843A>G