Canonical Allele Identifier: PA179220
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166297
ClinVar RCV Id: RCV000152482 RCV001134878 RCV000861721 RCV001134874 RCV001134875 RCV001134876 RCV001134877 RCV001171058 RCV004544380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gln3162Arg
CA179217
NM_133378.4:c.9485A>G