Canonical Allele Identifier: PA2826414409
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46791
ClinVar RCV Id: RCV000040061 RCV000227647 RCV000725243 RCV001170860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn8662His
CA139198
NM_001256850.1:c.25984A>C