Allele Registry

Canonical Allele Identifier: PA2830218004

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000439903

ClinVar Variation:

388627

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Asp13114Tyr	CA16604132 NM_133432.3:c.39340G>T