Canonical Allele Identifier: PA178387
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165664
ClinVar RCV Id: RCV000152165 RCV000277427 RCV000328826 RCV000324927 RCV000381891 RCV000376472 RCV000621516 RCV000471295 RCV000768836 RCV000724741 RCV000764299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val33467Gly
CA178384
NM_001267550.2:c.100400T>G