Canonical Allele Identifier: PA179352
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166325
ClinVar RCV Id: RCV000152511 RCV000172730 RCV000476516 RCV001133208 RCV001133210 RCV001133207 RCV001133209 RCV001133206 RCV001798487 RCV002460048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val1202Ala
CA179349
NM_001267550.2:c.3605T>C