Canonical Allele Identifier: PA2829435435
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val10821Gly
CA310149
NM_003319.4:c.32462T>G