Canonical Allele Identifier: PA178392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165678
ClinVar RCV Id: RCV000152169 RCV000462130 RCV000620518 RCV000764303 RCV001701771 RCV004532688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met30388Val
CA178391
NM_133378.4:c.91162A>G