Allele Registry

Canonical Allele Identifier: PA2830197691

Gene: TTN HGNC NCBI

ClinVar Allele:

496638

ClinVar RCV:

RCV000616686

ClinVar Variation:

517474

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Gly18827Ala	CA1991938 NM_133378.4:c.56480G>C