Canonical Allele Identifier: PA210949
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Arg486Cys
CA210948
NM_004820.5:c.1456C>T