ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827397465
Gene: CYP19A1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
17815
ClinVar RCV Id:
RCV000019393
RCV000814400
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001334177.1:p.Arg435Cys
CA127454
NM_001347248.1:c.1303C>T