Allele Registry

Canonical Allele Identifier: PA139192

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040055

RCV000284411

RCV000289133

RCV000327811

RCV000333598

RCV000381135

RCV000488131

RCV001084221

ClinVar Variation:

46785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asn8891Ser	CA139188 NM_001267550.2:c.26672A>G