Canonical Allele Identifier: PA658820285
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502050
ClinVar RCV Id: RCV000592907 RCV001854101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Asn160Asp
CA4764200
NM_004820.5:c.478A>G