Canonical Allele Identifier: PA178712
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165968
ClinVar RCV Id: RCV000152300 RCV000533354 RCV000727413 RCV000768986 RCV002433661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr15892Ala
CA178711
NM_133378.4:c.47674A>G