Canonical Allele Identifier: PA2830221114
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn18313Ser
CA310659
NM_133432.3:c.54938A>G