Canonical Allele Identifier: PA2830202205
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala29216Val
CA349462688
NM_133378.4:c.87647C>T