Canonical Allele Identifier: PA2830198915
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala21543Pro
CA1990515
NM_133378.4:c.64627G>C