Canonical Allele Identifier: PA2830216661
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu10833Gly
CA140139
NM_133432.3:c.32498A>G