Allele Registry

Canonical Allele Identifier: PA2830193598

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000473059

RCV001704962

ClinVar Variation:

203354

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ser8122Arg	CA312130 NM_133378.4:c.24366C>G CA349440683 NM_133378.4:c.24366C>A CA349440696 NM_133378.4:c.24364A>C