Canonical Allele Identifier: PA915954537
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 12622
ClinVar RCV Id: RCV000013457 RCV000308514 RCV002054435 RCV003974820
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Amino-acid Alleles

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