Canonical Allele Identifier: PA2829440389
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202923
ClinVar RCV Id: RCV000764309 RCV001129923 RCV001129925 RCV001134957 RCV001170780 RCV001704921 RCV001129924 RCV001129926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val19064Phe
CA310701
NM_003319.4:c.57190G>T