Canonical Allele Identifier: PA141244
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47517
ClinVar RCV Id: RCV000040786 RCV000249101 RCV000768864 RCV001082069 RCV000714118 RCV001839724 RCV001839725 RCV001839726 RCV001839727 RCV004541192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn29005Ser
CA141241
NM_001256850.1:c.87014A>G