Canonical Allele Identifier: PA915957335
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 35977
ClinVar RCV Id: RCV000029633 RCV000271806 RCV000518202 RCV000874647 RCV001095249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Asn335Asp
CA213644
NM_001026213.1:c.1003A>G