Canonical Allele Identifier: PA139302
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_596869.4:p.Lys8817Gln
CA139299
NM_133378.4:c.26449A>C