Canonical Allele Identifier: PA2830223274
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1297569
ClinVar RCV Id: RCV001723337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn21706His
CA349495682
NM_133432.3:c.65116A>C