Canonical Allele Identifier: PA2830226988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466741
ClinVar RCV Id: RCV000526551 RCV000593816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val26263Ala
CA1985231
NM_133432.3:c.78788T>C