Allele Registry

Canonical Allele Identifier: PA2830195609

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001553767

ClinVar Variation:

1192282

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Lys13717Gln	CA1994733 NM_133378.4:c.41149A>C