Allele Registry

Canonical Allele Identifier: PA309757

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184499

RCV000622210

RCV000643131

RCV003137715

ClinVar Variation:

202613

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Thr13599Ile	CA309755 NM_001267550.2:c.40796C>T