Allele Registry

Canonical Allele Identifier: PA139898

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040332

RCV000642909

RCV001588858

ClinVar Variation:

47062

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asp14847Asn	CA139896 NM_133378.4:c.44539G>A