Canonical Allele Identifier: PA645381438
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332895
ClinVar RCV Id: RCV000280491 RCV000286021 RCV000322342 RCV000380400 RCV000377045 RCV002502288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr9093Cys
CA10612088
NM_133378.4:c.27278A>G