Allele Registry

Canonical Allele Identifier: PA2830209129

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001293058

RCV001879970

ClinVar Variation:

978730

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Thr32423Ala	CA1985330 NM_133378.4:c.97267A>G