Allele Registry

Canonical Allele Identifier: PA311296

Gene: TTN HGNC NCBI

ClinVar Variation Id: 203117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ser34198Arg	CA311295 NM_001256850.1:c.102594T>G CA349400210 NM_001256850.1:c.102594T>A CA349400215 NM_001256850.1:c.102592A>C