Allele Registry

Canonical Allele Identifier: PA140169

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040427

RCV000172654

RCV000472663

RCV000768977

RCV001132010

RCV001132952

RCV002321528

ClinVar Variation:

47157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asp20002Gly	CA140165 NM_001267550.2:c.60005A>G