Canonical Allele Identifier: PA2826428069
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_001243779.1:p.Asp32837Glu
CA1985604
NM_001256850.1:c.98511C>A
CA349414280
NM_001256850.1:c.98511C>G