Canonical Allele Identifier: PA2830200329
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202914
ClinVar RCV Id: RCV000222951 RCV000234626 RCV000725384 RCV004537556 RCV002227935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser25017Tyr
CA310674
NM_133378.4:c.75050C>A