Canonical Allele Identifier: PA141979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47819
ClinVar RCV Id: RCV000041088 RCV000476484 RCV000727750 RCV002453334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala4061Thr
CA141976
NM_001267550.2:c.12181G>A