Allele Registry

Canonical Allele Identifier: PA181907

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000154986

RCV000726949

RCV001087945

ClinVar Variation:

178247

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asp6355Tyr	CA181905 NM_001267550.2:c.19063G>T