Allele Registry

Canonical Allele Identifier: PA2830203526

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000557315

ClinVar Variation:

466705

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Gly31660Arg	CA1985719 NM_133378.4:c.94978G>C