Canonical Allele Identifier: PA2830191054
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile1595Ser
CA60978210
NM_133378.4:c.4784T>G