Allele Registry

Canonical Allele Identifier: PA139290

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000040094

RCV000643692

RCV000725042

ClinVar Variation:

46824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Thr869Ser	CA139287 NM_001256850.1:c.2605A>T CA349496328 NM_001256850.1:c.2606C>G