Canonical Allele Identifier: PA2830200328
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332757
ClinVar RCV Id: RCV000314233 RCV000336400 RCV000356273 RCV000406935 RCV000406888 RCV000592500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys25010Glu
CA1989024
NM_133378.4:c.75028A>G