Canonical Allele Identifier: PA658665384
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467081
ClinVar RCV Id: RCV000535137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys12499Thr
CA349484207
NM_001267550.2:c.37496A>C