Allele Registry

Canonical Allele Identifier: PA2830201916

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000594645

RCV000643852

ClinVar Variation:

497027

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Asn28622Lys	CA1987281 NM_133378.4:c.85866T>A CA349482231 NM_133378.4:c.85866T>G