Canonical Allele Identifier: PA232150
Gene: CYP7A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 91913
ClinVar RCV Id: RCV000122470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000771.2:p.Arg303Trp
CA232149
NM_000780.4:c.907A>T