Canonical Allele Identifier: PA2829435375
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu10708Gly
CA140139
NM_003319.4:c.32123A>G