Canonical Allele Identifier: PA178452
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165761
ClinVar RCV Id: RCV000152193 RCV000172210 RCV000532604 RCV000765549 RCV003149922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29673Gln
CA178450
NM_001267550.2:c.89018G>A