Allele Registry

Canonical Allele Identifier: PA2826420435

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000439903

ClinVar Variation:

388627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Asp20413Tyr	CA16604132 NM_001256850.1:c.61237G>T