Canonical Allele Identifier: PA182008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178275
ClinVar RCV Id: RCV000155016 RCV000172492 RCV000266151 RCV000300150 RCV000305734 RCV000345372 RCV000358208 RCV000643424 RCV002399548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala529Thr
CA182006
NM_001267550.2:c.1585G>A