Canonical Allele Identifier: PA645382025
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405122
ClinVar RCV Id: RCV000462708 RCV001653822
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val307Met
CA2006172
NM_133379.5:c.919G>A