Canonical Allele Identifier: PA2580116739
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071592
ClinVar RCV Id: RCV002975700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Phe73Leu
CA350576797
NM_000784.4:c.217T>C
CA350576820
NM_000784.4:c.219C>G
CA350576824
NM_000784.4:c.219C>A