Canonical Allele Identifier: PA913200990
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_001254479.2:p.Asp32018Glu
CA60970431
NM_001267550.2:c.96054T>G
CA349454209
NM_001267550.2:c.96054T>A