Canonical Allele Identifier: PA2830227032
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 262342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala26306Gly
CA1985217
NM_133432.3:c.78917C>G