Canonical Allele Identifier: PA916065342
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.His6039Tyr
CA1995587
NM_133437.4:c.18115C>T