Canonical Allele Identifier: PA141950
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47809
ClinVar RCV Id: RCV000041078 RCV000539120 RCV000769095 RCV001719777 RCV004541203 RCV002390177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val3598Met
CA141947
NM_133432.3:c.10792G>A