Canonical Allele Identifier: PA2830213510
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46956
ClinVar RCV Id: RCV000040226 RCV000254284 RCV000458956 RCV000726937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met5230Thr
CA139622
NM_133432.3:c.15689T>C