Canonical Allele Identifier: PA2827397671
Gene: CYP19A1 HGNC NCBI
ClinVar RCV:
RCV000019396
ClinVar Variation:
17818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334178.1:p.Arg375Cys
CA127458
NM_001347249.1:c.1123C>T