Canonical Allele Identifier: PA140582
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47286
ClinVar RCV Id: RCV000040556 RCV000184775 RCV000544602 RCV001130762 RCV001130763 RCV001130764 RCV001133729 RCV001133730 RCV002326752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly23498Ser
CA140578
NM_001267550.2:c.70492G>A