Canonical Allele Identifier: PA2829439971
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47411
ClinVar RCV Id: RCV000040681 RCV000300172 RCV000322064 RCV000353764 RCV000456607 RCV000768905 RCV000357436 RCV000997376 RCV002345318 RCV000787943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys18403Gln
CA140922
NM_003319.4:c.55207A>C