Canonical Allele Identifier: PA238071
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192000
ClinVar RCV Id: RCV000172370 RCV001130655 RCV001130656 RCV001130657 RCV001130658 RCV001133624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala9561Thr
CA238069
NM_001267550.2:c.28681G>A