Allele Registry

Canonical Allele Identifier: PA309078

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000184159

RCV000538779

ClinVar Variation:

202320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Val22373Asp	CA309076 NM_001267550.2:c.67118T>A