Canonical Allele Identifier: PA2830208771
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202619
ClinVar RCV Id: RCV000184506 RCV000309772 RCV000343809 RCV000392746 RCV000370464 RCV000399409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val11242Met
CA309775
NM_133378.4:c.33724G>A