Canonical Allele Identifier: PA2830219861
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile16181Val
CA310511
NM_133432.3:c.48541A>G