Canonical Allele Identifier: PA210248
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 208947
ClinVar RCV Id: RCV000201427 RCV000642920 RCV003486764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val351Met
CA210245
NM_133379.5:c.1051G>A