Canonical Allele Identifier: PA645412312
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229551
ClinVar RCV Id: RCV000222441 RCV000525107 RCV000766676 RCV001130880 RCV001130881 RCV001133849 RCV001133850 RCV001130879 RCV002365162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro32400Thr
CA1986597
NM_001267550.2:c.97198C>A