Canonical Allele Identifier: PA311161
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203074
ClinVar RCV Id: RCV000223175 RCV000466888 RCV000727452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32996Trp
CA311160
NM_001256850.1:c.98986C>T