Canonical Allele Identifier: PA178522
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165851
ClinVar RCV Id: RCV000152222 RCV000643884 RCV000184785 RCV000617839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly23870Ser
CA178519
NM_001267550.2:c.71608G>A