Allele Registry

Canonical Allele Identifier: PA2830212847

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000316148

ClinVar Variation:

289447

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Gln3977Pro	CA10606447 NM_133432.3:c.11930A>C