Canonical Allele Identifier: PA2829435973
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Tyr11791Cys
CA1992209
NM_003319.4:c.35372A>G