Canonical Allele Identifier: PA645412465
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281787
ClinVar RCV Id: RCV000276620 RCV000282308 RCV000322337 RCV000331733 RCV000386284 RCV000373215 RCV000540534 RCV001170524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser32915Gly
CA1986314
NM_001267550.2:c.98743A>G