Canonical Allele Identifier: PA2830218451
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_597676.3:p.Asp13826Glu
CA1991145
NM_133432.3:c.41478C>A
CA349673184
NM_133432.3:c.41478C>G