Allele Registry

Canonical Allele Identifier: PA109991

Gene: PRDM16 HGNC NCBI

ClinVar RCV:

RCV000054522

RCV001239707

RCV001375649

ClinVar Variation:

60728

HGVS (amino-acid)	Matching Registered Transcripts
NP_071397.3:p.Pro291Leu	CA144646 NM_022114.4:c.872C>T