Allele Registry

Canonical Allele Identifier: PA2830204121

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV001704939

RCV001852407

ClinVar Variation:

203086

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Ser32364Arg	CA311196 NM_133378.4:c.97092T>G CA349410905 NM_133378.4:c.97092T>A CA349410910 NM_133378.4:c.97090A>C