Canonical Allele Identifier: PA2830222813
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499307
ClinVar RCV Id: RCV000643405 RCV000714112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu20980Asp
CA1987872
NM_133432.3:c.62940A>C
CA349516193
NM_133432.3:c.62940A>T