Canonical Allele Identifier: PA101595
Gene: CYP19A1 HGNC NCBI
ClinVar RCV:
RCV000019394
ClinVar Variation:
17816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000094.2:p.Cys437Tyr
CA127456
NM_000103.4:c.1310G>A