Canonical Allele Identifier: PA2830192627
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466879
ClinVar RCV Id: RCV000556465 RCV000595473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn5578Ser
CA2001214
NM_133378.4:c.16733A>G