Canonical Allele Identifier: PA283043
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46818
ClinVar RCV Id: RCV000040088 RCV000242546 RCV000270874 RCV000290670 RCV000329733 RCV000385212 RCV000388876 RCV001510182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile8474Thr
CA283041
NM_133378.4:c.25421T>C