Canonical Allele Identifier: PA235041
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167759
ClinVar RCV Id: RCV000154035 RCV000460324 RCV000723859 RCV002372006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32352His
CA235039
NM_001267550.2:c.97055G>A