Canonical Allele Identifier: PA211234
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178157
ClinVar RCV Id: RCV000119019 RCV000154875 RCV000713953 RCV000509179 RCV000852776 RCV000621822 RCV001134221 RCV001086721 RCV001134222 RCV001134223 RCV001798505 RCV004544417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32450Trp
CA211232
NM_001256850.1:c.97348C>T