Canonical Allele Identifier: PA2830206498
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332782
ClinVar RCV Id: RCV000264049 RCV000268546 RCV000316644 RCV000359836 RCV000373706 RCV003137946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp22485Ser
CA1990091
NM_133378.4:c.67454G>C