Canonical Allele Identifier: PA2830235089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile14415Met
CA178543
NM_133437.4:c.43245A>G