Canonical Allele Identifier: PA139081
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46738
ClinVar RCV Id: RCV000040008 RCV000643239 RCV001531338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gln6969His
CA139079
NM_133378.4:c.20907A>C
CA349497838
NM_133378.4:c.20907A>T