Canonical Allele Identifier: PA2829439830
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn18188Ser
CA310659
NM_003319.4:c.54563A>G