Canonical Allele Identifier: PA916066011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala7407Thr
CA1994738
NM_133437.4:c.22219G>A