Allele Registry

Canonical Allele Identifier: PA2826422192

Gene: TTN HGNC NCBI

ClinVar Variation Id: 178189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ser23527Arg	CA181717 NM_001256850.1:c.70581T>G CA349624719 NM_001256850.1:c.70581T>A CA349624741 NM_001256850.1:c.70579A>C