Canonical Allele Identifier: PA112621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178155
ClinVar RCV Id: RCV000154872 RCV000734113 RCV002483344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32996Gln
CA181570
NM_001256850.1:c.98987G>A