Canonical Allele Identifier: PA2830221462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502205
ClinVar RCV Id: RCV000595985 RCV001130883 RCV001130885 RCV001130887 RCV001130884 RCV001130886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr18844Met
CA1988932
NM_133432.3:c.56531C>T