Canonical Allele Identifier: PA891855444
Gene: BRWD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 585143
ClinVar RCV Id: RCV000709959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_387505.1:p.His1302Tyr
CA10026809
NM_033656.4:c.3904C>T