Canonical Allele Identifier: PA181871
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_001243779.1:p.Gly8623Ser
CA181869
NM_001256850.1:c.25867G>A