Canonical Allele Identifier: PA2830195655
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405004
ClinVar RCV Id: RCV000475726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala13824Glu
CA1994660
NM_133378.4:c.41471C>A