Canonical Allele Identifier: PA2830204050
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser32287Tyr
CA10613205
NM_133378.4:c.96860C>A