Canonical Allele Identifier: PA309903
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_001243779.1:p.Asp14359His
CA309902
NM_001256850.1:c.43075G>C