Canonical Allele Identifier: PA2830202757
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser30347Gly
CA1986314
NM_133378.4:c.91039A>G