Allele Registry

Canonical Allele Identifier: PA2830192331

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000185352

RCV000231532

RCV000299916

RCV000305709

RCV000345779

RCV000395936

RCV000401300

RCV000852906

ClinVar Variation:

203264

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Gln4713His	CA311856 NM_133378.4:c.14139A>T CA349568899 NM_133378.4:c.14139A>C