Canonical Allele Identifier: PA139899
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_001254479.2:p.Asp17415Asn
CA139896
NM_001267550.2:c.52243G>A