Canonical Allele Identifier: PA2830210007
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1780433
ClinVar RCV Id: RCV002410026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met601Thr
CA349505971
NM_133432.3:c.1802T>C