Canonical Allele Identifier: PA2830217071
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167776
ClinVar RCV Id: RCV000154061 RCV000723796 RCV001131520 RCV001131519 RCV001131521 RCV001131518 RCV001134510 RCV002453505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg11579Gln
CA235093
NM_133432.3:c.34736G>A