Canonical Allele Identifier: PA138793
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46625
ClinVar RCV Id: RCV000039895 RCV000205655 RCV000852907 RCV000725312 RCV001133898 RCV001133899 RCV001133900 RCV001130952 RCV001133901 RCV001798130 RCV004534857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu4498Phe
CA138791
NM_133378.4:c.13492C>T