Allele Registry

Canonical Allele Identifier: PA110000

Gene: PRDM16 HGNC NCBI

ClinVar RCV:

RCV000054521

RCV000204421

RCV000223010

RCV001610340

ClinVar Variation:

60727

HGVS (amino-acid)	Matching Registered Transcripts
NP_071397.3:p.Val1101Met	CA144645 NM_022114.4:c.3301G>A