Allele Registry

Canonical Allele Identifier: PA309936

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184574

ClinVar Variation:

202671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Gly14643Glu	CA309935 NM_001256850.1:c.43928G>A