Canonical Allele Identifier: PA645412974
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284110
ClinVar RCV Id: RCV000380276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp35965Gly
CA10604691
NM_001267550.2:c.107894A>G