Canonical Allele Identifier: PA178628
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165911
ClinVar RCV Id: RCV000152262 RCV000981791 RCV003137654 RCV002453495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg18454His
CA178627
NM_133378.4:c.55361G>A