Canonical Allele Identifier: PA2830233590
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Tyr11983Cys
CA1992209
NM_133437.4:c.35948A>G