Canonical Allele Identifier: PA178872
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166080
ClinVar RCV Id: RCV000152359 RCV000172670 RCV001086600 RCV001129205 RCV001131897 RCV001129202 RCV001129203 RCV001129204 RCV003486680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala10796Val
CA178871
NM_133378.4:c.32387C>T