Canonical Allele Identifier: PA2830202370
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_596869.4:p.Ala29519Gly
CA349450843
NM_133378.4:c.88556C>G