Canonical Allele Identifier: PA2830236518
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile16857Val
CA310560
NM_133437.4:c.50569A>G