Canonical Allele Identifier: PA238271
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192078
ClinVar RCV Id: RCV000172470 RCV000471938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His1952Arg
CA238269
NM_001267550.2:c.5855A>G