Canonical Allele Identifier: PA2830224299
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598664
ClinVar RCV Id: RCV000735113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala23147Gly
CA349450843
NM_133432.3:c.69440C>G