Canonical Allele Identifier: PA282792
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46679
ClinVar RCV Id: RCV000039949 RCV000713983 RCV001081389 RCV001136098 RCV001136099 RCV001136095 RCV001136096 RCV001136097 RCV003486573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile7007Phe
CA282788
NM_001267550.2:c.21019A>T