Canonical Allele Identifier: PA2830224858
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val23969Ala
CA141489
NM_133432.3:c.71906T>C