Allele Registry

Canonical Allele Identifier: PA138947

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000039953

RCV000082370

RCV000275531

RCV000278937

RCV000333001

RCV000367843

RCV000389765

RCV001079235

RCV001170083

ClinVar Variation:

46683

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ala5878Thr	CA138945 NM_133378.4:c.17632G>A