Canonical Allele Identifier: PA916065702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332855
ClinVar RCV Id: RCV000266276 RCV000310773 RCV000321133 RCV000361890 RCV000365565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr6928Ile
CA1995050
NM_133437.4:c.20783C>T