Canonical Allele Identifier: PA2830215758
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn9253Ser
CA1993613
NM_133432.3:c.27758A>G