Canonical Allele Identifier: PA2830198316
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404898
ClinVar RCV Id: RCV000474985 RCV000765555 RCV000997414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp20198Glu
CA1991145
NM_133378.4:c.60594C>A
CA349673184
NM_133378.4:c.60594C>G