Canonical Allele Identifier: PA2829432858
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405183
ClinVar RCV Id: RCV000465470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg6132Gly
CA1995414
NM_003319.4:c.18394A>G