ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828285946
Gene: CYP21A2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000012934
RCV000012935
RCV000012936
RCV000055820
RCV000210728
RCV000711385
RCV001804725
RCV003407320
ClinVar Variation:
12151
65610
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001355072.1:p.Val147Leu
CA121919
NM_001368143.1:c.439G>T
CA344933
NM_001368143.1:c.439G>C