Allele Registry

Canonical Allele Identifier: PA2830214682

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000525649

ClinVar Variation:

467208

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Pro7348Ser	CA60987700 NM_133432.3:c.22042C>T