Allele Registry

Canonical Allele Identifier: PA311197

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001704939

RCV001852407

ClinVar Variation:

203086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Ser33291Arg	CA311196 NM_001256850.1:c.99873T>G CA349410905 NM_001256850.1:c.99873T>A CA349410910 NM_001256850.1:c.99871A>C