Canonical Allele Identifier: PA2830202988
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405084
ClinVar RCV Id: RCV000462926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys30830Asn
CA16610218
NM_133378.4:c.92490A>T
CA349426552
NM_133378.4:c.92490A>C