Canonical Allele Identifier: PA310873
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202978
ClinVar RCV Id: RCV000284310 RCV000339329 RCV000274131 RCV000347762 RCV000457893 RCV000288065 RCV000394225 RCV000725303 RCV002362957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly28810Asp
CA310872
NM_001256850.1:c.86429G>A