Canonical Allele Identifier: PA2830200979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala26542Val
CA1988331
NM_133378.4:c.79625C>T