Canonical Allele Identifier: PA916065321
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229437
ClinVar RCV Id: RCV000216762 RCV000284481 RCV000380150 RCV000286745 RCV000341707 RCV000401971 RCV000534179 RCV001722171 RCV001798708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu5992Lys
CA1995603
NM_133437.4:c.17974G>A