Canonical Allele Identifier: PA2826420222
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1034245
ClinVar RCV Id: RCV001336916
ClinVar Variation Id: 1254129
ClinVar RCV Id: RCV001799111 RCV001665273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly20047Arg
CA1991786
NM_001256850.1:c.60139G>C
CA1991787
NM_001256850.1:c.60139G>A