Canonical Allele Identifier: PA238017
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13079Ile
CA238015
NM_001267550.2:c.39235G>A