Canonical Allele Identifier: PA237727
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191861
ClinVar RCV Id: RCV000172211 RCV002354434 RCV002478554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr29596Ser
CA237725
NM_001267550.2:c.88787C>G
CA349524843
NM_001267550.2:c.88786A>T