Allele Registry

Canonical Allele Identifier: PA312042

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000643054

RCV001130659

RCV001130660

RCV001130661

RCV001130662

RCV001130663

RCV001721184

ClinVar Variation:

203324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Ala7860Thr	CA312040 NM_001267550.2:c.23578G>A