Canonical Allele Identifier: PA181989
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178271
ClinVar RCV Id: RCV000155012 RCV000643286 RCV001704127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg1421Trp
CA181985
NM_133379.5:c.4261C>T