Allele Registry

Canonical Allele Identifier: PA309934

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184573

ClinVar Variation:

202670

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Pro16256Thr	CA309932 NM_001267550.2:c.48766C>A