Canonical Allele Identifier: PA2830209294
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32802Ala
CA60953427
NM_133378.4:c.98404A>G