Canonical Allele Identifier: PA2826671925
Gene: GON4L HGNC NCBI

Linked Data

ClinVar Variation Id: 487779
ClinVar RCV Id: RCV000577846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269787.1:p.Asn819Asp
CA342791923
NM_001282858.2:c.2455A>G