Allele Registry

Canonical Allele Identifier: PA309978

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000184590

RCV000327937

RCV000458919

RCV001133611

RCV001133612

RCV001133613

RCV001135102

RCV001135103

RCV002444752

ClinVar Variation:

202685

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ile15266Val	CA309977 NM_001256850.1:c.45796A>G