Canonical Allele Identifier: PA345168
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65837
ClinVar RCV Id: RCV000056077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Asn403Lys
CA345167
NM_000784.4:c.1209C>G
CA350593104
NM_000784.4:c.1209C>A