Canonical Allele Identifier: PA2830227754
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 425238
ClinVar RCV Id: RCV000488335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile27046Val
CA16621775
NM_133432.3:c.81136A>G