Canonical Allele Identifier: PA645412614
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229561
ClinVar RCV Id: RCV000220026 RCV000466841 RCV000730725 RCV000769858 RCV002381750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp33793Val
CA1985896
NM_001267550.2:c.101378A>T