Canonical Allele Identifier: PA2830197432
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp18243Gly
CA310206
NM_133378.4:c.54728A>G