Allele Registry

Canonical Allele Identifier: PA311487

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000538379

RCV001704945

RCV002390484

ClinVar Variation:

203155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ile2586Met	CA311485 NM_001256850.1:c.7758A>G