Canonical Allele Identifier: PA139301
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46829
ClinVar RCV Id: RCV000040099 RCV000468986 RCV000768894 RCV001703899 RCV004541142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys10061Gln
CA139299
NM_001267550.2:c.30181A>C