Canonical Allele Identifier: PA2741849695
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2933743
ClinVar RCV Id: RCV003793301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35340Ala
CA349407207
NM_001267550.2:c.106019G>C