Allele Registry

Canonical Allele Identifier: PA139190

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040055

RCV000284411

RCV000289133

RCV000327811

RCV000333598

RCV000381135

RCV000488131

RCV001084221

ClinVar Variation:

46785

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asn7647Ser	CA139188 NM_133378.4:c.22940A>G