Canonical Allele Identifier: PA181870
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178234
ClinVar RCV Id: RCV000154970 RCV000172685 RCV001083461 RCV001131297 RCV001131296 RCV001130564 RCV001131298 RCV001131299 RCV004544428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly7696Ser
CA181869
NM_133378.4:c.23086G>A