Canonical Allele Identifier: PA182005
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178274
ClinVar RCV Id: RCV000155015 RCV000550907 RCV000727539 RCV001293183 RCV002444639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr799Met
CA182001
NM_133379.5:c.2396C>T