Canonical Allele Identifier: PA2830206009
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val14515Phe
CA310001
NM_133378.4:c.43543G>T