Canonical Allele Identifier: PA2829436153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47194
ClinVar RCV Id: RCV000040464 RCV000172292 RCV000248255 RCV000269467 RCV000332764 RCV000328753 RCV000367338 RCV000382596 RCV000852826 RCV001080206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg12053Trp
CA140280
NM_003319.4:c.36157C>T