Canonical Allele Identifier: PA140859
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47386
ClinVar RCV Id: RCV000040656 RCV000154047 RCV000242849 RCV000471525 RCV000852499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly25168Ser
CA140856
NM_001256850.1:c.75502G>A