Canonical Allele Identifier: PA2830221675
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn19193Ser
CA184934
NM_133432.3:c.57578A>G