Canonical Allele Identifier: PA2830210929
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile1549Ser
CA60978210
NM_133432.3:c.4646T>G