Canonical Allele Identifier: PA2826492568
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile1595Ser
CA60978210
NM_001267550.2:c.4784T>G