Canonical Allele Identifier: PA302914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196150
ClinVar RCV Id: RCV000219348 RCV000542576 RCV000724710 RCV001293052 RCV002354453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly26994Asp
CA302913
NM_133378.4:c.80981G>A