Canonical Allele Identifier: PA312069
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203333
ClinVar RCV Id: RCV000185441 RCV000468163 RCV001136403 RCV001136404 RCV001136400 RCV001136402 RCV001136401 RCV001293230 RCV004539730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg8356Cys
CA312067
NM_001267550.2:c.25066C>T