Allele Registry

Canonical Allele Identifier: PA183468

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000155780

RCV000172245

RCV000254311

RCV000291098

RCV000316713

RCV000330851

RCV000371276

RCV000385420

RCV001078567

RCV001170788

RCV001293186

ClinVar Variation:

179002

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Thr24385Met	CA183467 NM_133378.4:c.73154C>T