Canonical Allele Identifier: PA2830226611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser25915Tyr
CA10613205
NM_133432.3:c.77744C>A