Canonical Allele Identifier: PA2830210425
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val999Met
CA139502
NM_133432.3:c.2995G>A