Canonical Allele Identifier: PA2830210696
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229444
ClinVar RCV Id: RCV000221874 RCV000532189 RCV000617303 RCV001697190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile1315Leu
CA2005411
NM_133432.3:c.3943A>C