Allele Registry

Canonical Allele Identifier: PA2826416920

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000541917

RCV001564240

RCV002413549

ClinVar Variation:

467181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Gly13890Arg	CA1995217 NM_001256850.1:c.41668G>A CA60991509 NM_001256850.1:c.41668G>C