Canonical Allele Identifier: PA2830243512
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466750
ClinVar RCV Id: RCV000547265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp26523Glu
CA349406705
NM_133437.4:c.79569T>G
CA349406709
NM_133437.4:c.79569T>A