Canonical Allele Identifier: PA2573173786
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1381185
ClinVar RCV Id: RCV001895236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Cys476Tyr
CA350595186
NM_000784.4:c.1427G>A