Canonical Allele Identifier: PA181847
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178228
ClinVar RCV Id: RCV000154963 RCV000724173 RCV001087214
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala9447Thr
CA181845
NM_133378.4:c.28339G>A