Canonical Allele Identifier: PA309913
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202663
ClinVar RCV Id: RCV000184566 RCV000227076 RCV000254392 RCV001704899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16055His
CA309911
NM_001267550.2:c.48164G>A