Allele Registry

Canonical Allele Identifier: PA109961

Gene: PRDM16 HGNC NCBI

ClinVar RCV:

RCV000054520

RCV000853165

ClinVar Variation:

60726

HGVS (amino-acid)	Matching Registered Transcripts
NP_071397.3:p.Asn816Ser	CA144644 NM_022114.4:c.2447A>G