Canonical Allele Identifier: PA141088
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47464
ClinVar RCV Id: RCV000040733 RCV000172625 RCV000618830 RCV001086492 RCV001129292 RCV001129291 RCV001131993 RCV001131994 RCV001131995 RCV001293177 RCV001798189 RCV002227443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro29138Thr
CA141084
NM_001267550.2:c.87412C>A