Canonical Allele Identifier: PA2830238856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Leu20626Arg
CA310778
NM_133437.4:c.61877T>G