Canonical Allele Identifier: PA183469
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179002
ClinVar RCV Id: RCV000155780 RCV000172245 RCV000254311 RCV000291098 RCV000316713 RCV000330851 RCV000385420 RCV000371276 RCV001078567 RCV001170788 RCV001293186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr25312Met
CA183467
NM_001256850.1:c.75935C>T