Allele Registry

Canonical Allele Identifier: PA645410663

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000439903

ClinVar Variation:

388627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Asp22054Tyr	CA16604132 NM_001267550.2:c.66160G>T