Canonical Allele Identifier: PA139898
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47062
ClinVar RCV Id: RCV000040332 RCV000642909 RCV001588858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp14847Asn
CA139896
NM_133378.4:c.44539G>A