Canonical Allele Identifier: PA310465
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202845
ClinVar RCV Id: RCV000472425 RCV001704917 RCV002336482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr24276Ser
CA310463
NM_001267550.2:c.72826A>T
CA349645266
NM_001267550.2:c.72827C>G