Allele Registry

Canonical Allele Identifier: PA138876

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000039923

RCV000154091

RCV000769064

RCV001086633

RCV001134662

RCV001134663

RCV001134664

RCV001134665

RCV001134666

RCV004534862

ClinVar Variation:

46653

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Pro6384Thr	CA138872 NM_001267550.2:c.19150C>A