Canonical Allele Identifier: PA345180
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65850
ClinVar RCV Id: RCV000056090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Pro468Ser
CA345179
NM_000784.4:c.1402C>T