Canonical Allele Identifier: PA309925
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202667
ClinVar RCV Id: RCV000460733 RCV000769000 RCV001704900 RCV002265671 RCV002415795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn16170Ser
CA309923
NM_001267550.2:c.48509A>G