Canonical Allele Identifier: PA181621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96315
ClinVar RCV Id: RCV000154889 RCV000463812 RCV001727567 RCV004529868 RCV002362733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31428His
CA181617
NM_001267550.2:c.94283G>A