Allele Registry

Canonical Allele Identifier: PA178862

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000152356

RCV000556771

RCV001719941

RCV002381478

ClinVar Variation:

166074

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ala11067Thr	CA178861 NM_133378.4:c.33199G>A