Canonical Allele Identifier: PA237637
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191823
ClinVar RCV Id: RCV000172164 RCV001087093 RCV004539583 RCV003319184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33903His
CA237635
NM_001267550.2:c.101708G>A