Allele Registry

Canonical Allele Identifier: PA141996

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000041097

RCV000725423

RCV000770111

ClinVar Variation:

47828

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Ile3980Thr	CA141993 NM_133432.3:c.11939T>C