Canonical Allele Identifier: PA2826429029
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466750
ClinVar RCV Id: RCV000547265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp33755Glu
CA349406705
NM_001256850.1:c.101265T>G
CA349406709
NM_001256850.1:c.101265T>A