Canonical Allele Identifier: PA289088
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130663
ClinVar RCV Id: RCV000118737 RCV000227944 RCV000229796 RCV001134163 RCV001134164 RCV001134165 RCV001134166 RCV001134167 RCV002381429 RCV004529987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val433Ile
CA289082
NM_133379.5:c.1297G>A