Canonical Allele Identifier: PA178657
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_596869.4:p.Thr16829Met
CA178656
NM_133378.4:c.50486C>T