Canonical Allele Identifier: PA2830226166
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229565
ClinVar RCV Id: RCV000217480 RCV000230688 RCV002223195 RCV002390586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp25538Glu
CA1985604
NM_133432.3:c.76614C>A
CA349414280
NM_133432.3:c.76614C>G