Canonical Allele Identifier: PA178778
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165992
ClinVar RCV Id: RCV000152326 RCV000250139 RCV000541819 RCV003137656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala17671Val
CA178776
NM_001267550.2:c.53012C>T