Allele Registry

Canonical Allele Identifier: PA135414

Gene: ESRRB HGNC NCBI

ClinVar Variation Id: 44997

HGVS (amino-acid)	Matching Registered Transcripts
NP_004443.3:p.Phe456Leu	CA135413 NM_004452.4:c.1366T>C CA390480068 NM_004452.4:c.1368C>A CA390480069 NM_004452.4:c.1368C>G