Allele Registry

Canonical Allele Identifier: PA139766

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040283

RCV000082410

RCV000299345

RCV000314422

RCV000349511

RCV000369133

RCV000406274

RCV000619989

RCV000852853

RCV001083906

RCV001798153

ClinVar Variation:

47013

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Pro15849Thr	CA139762 NM_001267550.2:c.47545C>A