Canonical Allele Identifier: PA645382742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332961
ClinVar RCV Id: RCV000286362 RCV000356189 RCV000341244 RCV000406971 RCV000406964 RCV003137958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala1081Val
CA2005593
NM_133379.5:c.3242C>T