Canonical Allele Identifier: PA2830216048
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn9723Ser
CA1993349
NM_133432.3:c.29168A>G