Canonical Allele Identifier: PA916065279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Lys5935Thr
CA1995649
NM_133437.4:c.17804A>C