Canonical Allele Identifier: PA645411010
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332782
ClinVar RCV Id: RCV000264049 RCV000268546 RCV000316644 RCV000359836 RCV000373706 RCV003137946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Trp25053Ser
CA1990091
NM_001267550.2:c.75158G>C