Allele Registry

Canonical Allele Identifier: PA138854

Gene: TTN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000039916

RCV000082364

RCV000262868

RCV000296922

RCV000302779

RCV000342596

RCV000355321

RCV000852901

RCV001082917

RCV001798131

ClinVar Variation:

46646

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asn5031Ser	CA138852 NM_133378.4:c.15092A>G