Canonical Allele Identifier: PA658680520
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191
ClinVar RCV Id: RCV000527993 RCV002497143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile1595Ser
CA60978210
NM_133379.5:c.4784T>G