Allele Registry

Canonical Allele Identifier: PA916066663

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040345

RCV000276975

RCV000278213

RCV000332004

RCV000366890

RCV000372745

RCV000560612

RCV000770011

RCV001719771

RCV002426579

RCV004534907

ClinVar Variation:

47075

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_597681.4:p.Phe8881Leu	CA139925 NM_133437.4:c.26641T>C CA349565645 NM_133437.4:c.26643T>G CA349565647 NM_133437.4:c.26643T>A