Canonical Allele Identifier: PA238137
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192026
ClinVar RCV Id: RCV000172403 RCV000535301 RCV001798617 RCV002225089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp5768Asn
CA238135
NM_001267550.2:c.17302G>A