Canonical Allele Identifier: PA312089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203340
ClinVar RCV Id: RCV000461658 RCV000725269 RCV003323436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly8301Glu
CA312088
NM_001256850.1:c.24902G>A