Canonical Allele Identifier: PA2830206827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr16204Ala
CA16610408
NM_133378.4:c.48610A>G