Canonical Allele Identifier: PA181926
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178253
ClinVar RCV Id: RCV000154993 RCV000468325 RCV000727723
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile5936Val
CA181923
NM_001267550.2:c.17806A>G