Canonical Allele Identifier: PA310867
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr28759Phe
CA310866
NM_001256850.1:c.86276A>T