Canonical Allele Identifier: PA2829430281
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile1549Ser
CA60978210
NM_003319.4:c.4646T>G