Canonical Allele Identifier: PA2826489471
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229504
ClinVar RCV Id: RCV000214672 RCV000461917 RCV001528592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp2140Glu
CA2005052
NM_001267550.2:c.6420T>A
CA349439525
NM_001267550.2:c.6420T>G