Canonical Allele Identifier: PA2830213567
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404688
ClinVar RCV Id: RCV000463928 RCV000604586 RCV000714032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp5340Glu
CA1996010
NM_133432.3:c.16020T>G
CA349653714
NM_133432.3:c.16020T>A