Canonical Allele Identifier: PA2826426095
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala30143Val
CA349462688
NM_001256850.1:c.90428C>T