Canonical Allele Identifier: PA2830205906
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val14357Ala
CA309980
NM_133378.4:c.43070T>C