Canonical Allele Identifier: PA185029
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179736
ClinVar RCV Id: RCV000156534 RCV000643144 RCV002345520
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser403Thr
CA185027
NM_001267550.2:c.1208G>C