Canonical Allele Identifier: PA2826421139
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165861
ClinVar RCV Id: RCV000152233 RCV000723936 RCV001130896 RCV001081781 RCV001130195 RCV001130196 RCV001130897 RCV001130898 RCV002326873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile21647Met
CA178543
NM_001256850.1:c.64941A>G