Canonical Allele Identifier: PA915982187
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238738
ClinVar RCV Id: RCV000226894 RCV000730580 RCV001170631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala9778Thr
CA1999195
NM_001256850.1:c.29332G>A