Allele Registry

Canonical Allele Identifier: PA309937

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184574

ClinVar Variation:

202671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Gly16284Glu	CA309935 NM_001267550.2:c.48851G>A