Canonical Allele Identifier: PA238328
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192094
ClinVar RCV Id: RCV000172487 RCV000557117 RCV001135137 RCV001135139 RCV001135141 RCV001135138 RCV001135140 RCV002426824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.His786Gln
CA238324
NM_133379.5:c.2358C>G
CA349499544
NM_133379.5:c.2358C>A