Allele Registry

Canonical Allele Identifier: PA179331

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000152506

RCV000172729

RCV000230032

RCV000769129

RCV000852937

RCV001131924

RCV001131925

RCV001131926

RCV001132892

RCV001132893

RCV002326877

ClinVar Variation:

166320

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Phe1466Leu	CA179328 NM_001267550.2:c.4396T>C CA349469144 NM_001267550.2:c.4398C>G CA349469147 NM_001267550.2:c.4398C>A