Canonical Allele Identifier: PA645411391
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_001254479.2:p.Lys27578Glu
CA1989024
NM_001267550.2:c.82732A>G