Canonical Allele Identifier: PA310779
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202948
ClinVar RCV Id: RCV000184934 RCV000725754 RCV000643904 RCV002354514
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu27858Arg
CA310778
NM_001256850.1:c.83573T>G