Canonical Allele Identifier: PA138892
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46663
ClinVar RCV Id: RCV000039933 RCV000643024 RCV001703895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp5411Asn
CA138890
NM_133378.4:c.16231G>A