Canonical Allele Identifier: PA2830227168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 512644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala26438Val
CA1985159
NM_133432.3:c.79313C>T