Canonical Allele Identifier: PA237726
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_596869.4:p.Thr27028Ser
CA237725
NM_133378.4:c.81083C>G
CA349524843
NM_133378.4:c.81082A>T