Canonical Allele Identifier: PA645410049
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229448
ClinVar RCV Id: RCV000222383 RCV000245655 RCV000533460 RCV001556216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly16881Ala
CA1994330
NM_001267550.2:c.50642G>C