Canonical Allele Identifier: PA2829437212
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47268
ClinVar RCV Id: RCV000040538 RCV000282806 RCV000307639 RCV000342426 RCV000337009 RCV000405692 RCV000463057 RCV000618829 RCV001093056 RCV001787841 RCV001293209 RCV001798175 RCV004534921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala13755Pro
CA140519
NM_003319.4:c.41263G>C