Canonical Allele Identifier: PA310562
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile25730Val
CA310560
NM_001267550.2:c.77188A>G