Allele Registry

Canonical Allele Identifier: PA141768

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000040986

RCV000538774

RCV000620414

RCV000726670

RCV001131606

RCV001131607

RCV001131608

RCV001131609

RCV001131610

RCV001171217

ClinVar Variation:

47717

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Arg34011Gln	CA141765 NM_001256850.1:c.102032G>A