Canonical Allele Identifier: PA178717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165969
ClinVar RCV Id: RCV000152301 RCV000172660 RCV000476468 RCV002433662 RCV001798480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser18458Arg
CA178714
NM_001267550.2:c.55374C>G
CA349541918
NM_001267550.2:c.55374C>A
CA349541938
NM_001267550.2:c.55372A>C