Canonical Allele Identifier: PA2580311986
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039922
ClinVar RCV Id: RCV002886125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Ile395Val
CA371334094
NM_004820.5:c.1183A>G