Canonical Allele Identifier: PA645410062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238795
ClinVar RCV Id: RCV000226574 RCV000764332 RCV001551023 RCV000618429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala17022Val
CA1994257
NM_001267550.2:c.51065C>T