Canonical Allele Identifier: PA178658
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165947
ClinVar RCV Id: RCV000152275 RCV000643314 RCV000723958 RCV003149926
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr19397Met
CA178656
NM_001267550.2:c.58190C>T