Canonical Allele Identifier: PA2580311960
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050175
ClinVar RCV Id: RCV002937482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Thr173Pro
CA4764193
NM_004820.5:c.517A>C