Canonical Allele Identifier: PA310868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr30400Phe
CA310866
NM_001267550.2:c.91199A>T