Canonical Allele Identifier: PA311858
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203264
ClinVar RCV Id: RCV000185352 RCV000299916 RCV000305709 RCV000345779 RCV000231532 RCV000401300 RCV000395936 RCV000852906
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln5957His
CA311856
NM_001267550.2:c.17871A>T
CA349568899
NM_001267550.2:c.17871A>C