Allele Registry

Canonical Allele Identifier: PA138660

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000039847

RCV000172723

RCV001081037

RCV001129648

RCV001129649

RCV001129650

RCV001129651

RCV001134674

RCV002381318

ClinVar Variation:

46577

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Arg3363His	CA138655 NM_133378.4:c.10088G>A