Canonical Allele Identifier: PA2830215914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr9520Ala
CA178711
NM_133432.3:c.28558A>G