Allele Registry

Canonical Allele Identifier: PA139672

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040242

RCV000463518

RCV000725048

RCV000852859

RCV001130917

RCV001130918

RCV001130919

RCV001130920

RCV001130921

RCV001171013

RCV002399389

ClinVar Variation:

46972

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ser11996Thr	CA139670 NM_133378.4:c.35986T>A