Canonical Allele Identifier: PA178878
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166082
ClinVar RCV Id: RCV000152360 RCV000228409 RCV001704102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu13193Gly
CA178875
NM_001267550.2:c.39578A>G