Canonical Allele Identifier: PA645408783
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 385539
ClinVar RCV Id: RCV000528151 RCV000730353 RCV002436297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala4111Gly
CA2002731
NM_001267550.2:c.12332C>G