Canonical Allele Identifier: PA302887
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196066
ClinVar RCV Id: RCV000259190 RCV000539580 RCV000769926 RCV000724797 RCV002345607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro24590Ala
CA302886
NM_133378.4:c.73768C>G