Canonical Allele Identifier: PA101568
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17821
ClinVar RCV Id: RCV000019399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000094.2:p.Arg365Gln
CA127460
NM_000103.4:c.1094G>A