Canonical Allele Identifier: PA913199911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 626696
ClinVar RCV Id: RCV000770110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu4247Gly
CA60984099
NM_001267550.2:c.12740A>G