Canonical Allele Identifier: PA2829434775
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn9598Ser
CA1993349
NM_003319.4:c.28793A>G