Allele Registry

Canonical Allele Identifier: PA140652

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040583

RCV000460260

RCV000620443

RCV000723985

ClinVar Variation:

47313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Met24061Thr	CA140649 NM_001267550.2:c.72182T>C