Canonical Allele Identifier: PA183600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179043
ClinVar RCV Id: RCV000155827 RCV000476685 RCV000733639 RCV000769975 RCV002345509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21604Gln
CA183598
NM_001267550.2:c.64811G>A