Allele Registry

Canonical Allele Identifier: PA184392

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000156208

RCV000248812

RCV000713993

RCV001083518

RCV001130359

RCV001130360

RCV001135405

RCV001135406

RCV001135407

RCV003486706

ClinVar Variation:

179419

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asp7675Tyr	CA184389 NM_001267550.2:c.23023G>T