Canonical Allele Identifier: PA913200992
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598664
ClinVar RCV Id: RCV000735113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala32087Gly
CA349450843
NM_001267550.2:c.96260C>G