Canonical Allele Identifier: PA355759
Gene: CYP7B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219384
ClinVar RCV Id: RCV000205382 RCV000512932 RCV001163749 RCV003955222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004811.1:p.Pro20Leu
CA349540
NM_004820.5:c.59C>T