Canonical Allele Identifier: PA097772
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6104
ClinVar RCV Id: RCV000006478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Phe216Ser
CA210943
NM_004820.5:c.647T>C