Allele Registry

Canonical Allele Identifier: PA915954537

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013457

RCV000308514

RCV002054435

RCV003974820

ClinVar Variation:

12622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Gly277Ser	CA122571 NM_001063.4:c.829G>A