Allele Registry

Canonical Allele Identifier: PA916066019

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000233666

ClinVar Variation:

224702

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Val7409Ala	CA10575971 NM_133437.4:c.22226T>C