Canonical Allele Identifier: PA916065814
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202660
ClinVar RCV Id: RCV000591920 RCV000621855 RCV001082934 RCV001128987 RCV001128984 RCV001128985 RCV001128986 RCV000725808 RCV001128988 RCV004537546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp7127His
CA309902
NM_133437.4:c.21379G>C