Allele Registry

Canonical Allele Identifier: PA141682

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040942

RCV000172455

RCV000544021

RCV000769101

RCV002371853

ClinVar Variation:

47673

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asn3225Ser	CA141678 NM_133378.4:c.9674A>G