Canonical Allele Identifier: PA2829445749
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 262342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala26181Gly
CA1985217
NM_003319.4:c.78542C>G