Allele Registry

Canonical Allele Identifier: PA210248

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000201427

RCV000642920

RCV003486764

ClinVar Variation:

208947

HGVS (amino-acid)	Matching Registered Transcripts
NP_596870.2:p.Val351Met	CA210245 NM_133379.5:c.1051G>A