Canonical Allele Identifier: PA2830215886
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47103
ClinVar RCV Id: RCV000040373 RCV000797680 RCV003156220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Lys9483Asn
CA140013
NM_133432.3:c.28449G>C
CA349543218
NM_133432.3:c.28449G>T