Allele Registry

Canonical Allele Identifier: PA2830234337

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000439903

ClinVar Variation:

388627

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Asp13181Tyr	CA16604132 NM_133437.4:c.39541G>T