Allele Registry

Canonical Allele Identifier: PA184842

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000156444

RCV000475607

RCV000620906

RCV001262303

RCV003137680

RCV003149957

RCV004535009

ClinVar Variation:

179648

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ala32186Val	CA184841 NM_133378.4:c.96557C>T