Allele Registry

Canonical Allele Identifier: PA141997

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000041097

RCV000725423

RCV000770111

ClinVar Variation:

47828

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ile4218Thr	CA141993 NM_001267550.2:c.12653T>C