Allele Registry

Canonical Allele Identifier: PA302613

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000172634

RCV000213073

RCV001086328

RCV001171262

RCV002225090

RCV002345598

ClinVar Variation:

192153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ala25739Gly	CA302610 NM_001267550.2:c.77216C>G