Canonical Allele Identifier: PA2499234142
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Lys353Asn
CA2112791
NM_000784.4:c.1059G>T
CA350591568
NM_000784.4:c.1059G>C