Canonical Allele Identifier: PA2830197851
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202793
ClinVar RCV Id: RCV000184726 RCV000262099 RCV000260739 RCV000302097 RCV000319553 RCV000358672 RCV000462751 RCV003137729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg19147Leu
CA310307
NM_133378.4:c.57440G>T