Canonical Allele Identifier: PA183581
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179037
ClinVar RCV Id: RCV000155821 RCV000415349 RCV000726977 RCV001129493 RCV001129494 RCV001086291 RCV001129490 RCV001129492 RCV001129491 RCV002362823 RCV003486700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys28700Thr
CA183580
NM_133378.4:c.86099A>C