Canonical Allele Identifier: PA658816486
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 513448
ClinVar RCV Id: RCV000614303 RCV000643213 RCV001129288 RCV001129290 RCV001129289 RCV001129286 RCV001129287 RCV001698079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met29200Ile
CA1988293
NM_001267550.2:c.87600G>C
CA349535308
NM_001267550.2:c.87600G>T
CA349535311
NM_001267550.2:c.87600G>A