Canonical Allele Identifier: PA2829441978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518580
ClinVar RCV Id: RCV000617373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr21568Ile
CA349496090
NM_003319.4:c.64703C>T