Canonical Allele Identifier: PA2829436829
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47238
ClinVar RCV Id: RCV000040508 RCV000473534 RCV000714072 RCV002371842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp13160Asn
CA140414
NM_003319.4:c.39478G>A