Canonical Allele Identifier: PA2830206872
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229466
ClinVar RCV Id: RCV000220952 RCV000544463 RCV000727258 RCV000764324 RCV003486775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr16277Pro
CA1993236
NM_133378.4:c.48829A>C