Canonical Allele Identifier: PA2826425355
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192200
ClinVar RCV Id: RCV000172785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn29005Asp
CA200064
NM_001256850.1:c.87013A>G