Allele Registry

Canonical Allele Identifier: PA2830207879

Gene: TTN HGNC NCBI

ClinVar Variation Id: 467349

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Tyr18288Cys	CA1992209 NM_133378.4:c.54863A>G