Canonical Allele Identifier: PA2829442923
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179890
ClinVar RCV Id: RCV000156691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gln22890Leu
CA185359
NM_003319.4:c.68669A>T