Allele Registry

Canonical Allele Identifier: PA138837

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000039912

RCV000545466

RCV000725041

ClinVar Variation:

46642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Glu6221Asp	CA138833 NM_001267550.2:c.18663A>C CA349560408 NM_001267550.2:c.18663A>T