Canonical Allele Identifier: PA2830221099
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn18284Ser
CA140891
NM_133432.3:c.54851A>G