Allele Registry

Canonical Allele Identifier: PA109979

Gene: PRDM16 HGNC NCBI

ClinVar RCV:

RCV000054523

ClinVar Variation:

60729

HGVS (amino-acid)	Matching Registered Transcripts
NP_071397.3:p.Leu887Pro	CA144647 NM_022114.4:c.2660T>C