Allele Registry

Canonical Allele Identifier: PA658665598

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000541917

RCV001564240

RCV002413549

ClinVar Variation:

467181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Gly15531Arg	CA1995217 NM_001267550.2:c.46591G>A CA60991509 NM_001267550.2:c.46591G>C