Canonical Allele Identifier: PA179214
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166296
ClinVar RCV Id: RCV000152481 RCV000643842 RCV002372002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser3271Ala
CA179212
NM_001267550.2:c.9811T>G