Canonical Allele Identifier: PA2830220569
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467520
ClinVar RCV Id: RCV000525632 RCV000768915 RCV001591240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu17477Asp
CA1989500
NM_133432.3:c.52431G>C
CA349598448
NM_133432.3:c.52431G>T