Allele Registry

Canonical Allele Identifier: PA178387

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000152165

RCV000277427

RCV000324927

RCV000328826

RCV000376472

RCV000381891

RCV000471295

RCV000621516

RCV000724741

RCV000764299

RCV000768836

ClinVar Variation:

165664

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Val33467Gly	CA178384 NM_001267550.2:c.100400T>G