Canonical Allele Identifier: PA916066098
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro7580Thr
CA1994613
NM_133437.4:c.22738C>A