Canonical Allele Identifier: PA178867
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166076
ClinVar RCV Id: RCV000152357 RCV002381479 RCV000725706 RCV001089127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg13501His
CA178865
NM_001267550.2:c.40502G>A