Canonical Allele Identifier: PA302590
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala89Gly
CA302585
NM_133379.5:c.266C>G