Canonical Allele Identifier: PA2830240592
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598666
ClinVar RCV Id: RCV000735115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp23145Glu
CA60970431
NM_133437.4:c.69435T>G
CA349454209
NM_133437.4:c.69435T>A