Allele Registry

Canonical Allele Identifier: PA645493072

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032176

ClinVar Variation:

38925

HGVS (amino-acid)	Matching Registered Transcripts
NP_036593.2:p.Phe288Leu	CA343189 NM_012461.2:c.862T>C CA389225356 NM_012461.2:c.864T>G CA389225360 NM_012461.2:c.864T>A