Canonical Allele Identifier: PA645381813
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332888
ClinVar RCV Id: RCV000303687 RCV000307184 RCV000342253 RCV000364327 RCV000398692 RCV000609781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile9717Val
CA10613118
NM_133378.4:c.29149A>G