Canonical Allele Identifier: PA178385
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_596869.4:p.Val30899Gly
CA178384
NM_133378.4:c.92696T>G