Canonical Allele Identifier: PA2830194284
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283437
ClinVar RCV Id: RCV000263993 RCV000458463 RCV000725270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu10497Asp
CA10604489
NM_133378.4:c.31491A>T
CA349496544
NM_133378.4:c.31491A>C