Allele Registry

Canonical Allele Identifier: PA915954567

Gene: TF HGNC NCBI

ClinVar Allele:

27656

ClinVar RCV:

RCV000013451

RCV000376325

RCV002054434

ClinVar Variation:

12617

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Pro589Ser	CA122563 NM_001063.4:c.1765C>T