Canonical Allele Identifier: PA645500185
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 309995
ClinVar RCV Id: RCV000321839 RCV001850635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Asn502Ser
CA6658109
NM_000785.4:c.1505A>G