Canonical Allele Identifier: PA2830233052
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val11013Gly
CA310149
NM_133437.4:c.33038T>G