Allele Registry

Canonical Allele Identifier: PA141725

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040955

RCV000230763

RCV001697033

RCV002381322

ClinVar Variation:

47686

HGVS (amino-acid)	Matching Registered Transcripts
NP_596870.2:p.Val3250Gly	CA141720 NM_133379.5:c.9749T>G