Canonical Allele Identifier: PA2830243492
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Phe26501Tyr
CA183679
NM_133437.4:c.79502T>A