Canonical Allele Identifier: PA658680669
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467487
ClinVar RCV Id: RCV000526249 RCV003486871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr2545Ile
CA61006134
NM_133379.5:c.7634C>T