Canonical Allele Identifier: PA2830234043
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96296
ClinVar RCV Id: RCV000154930 RCV000272166 RCV000381758 RCV000329528 RCV000468946 RCV000289674 RCV000342201 RCV000619243 RCV000852823 RCV001798281 RCV001811388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly12715Arg
CA181752
NM_133437.4:c.38143G>A
CA349436974
NM_133437.4:c.38143G>C