Canonical Allele Identifier: PA645499753
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 260999
ClinVar RCV Id: RCV000243801 RCV000262444 RCV002401960 RCV001516491
ClinVar Variation Id: 1169853
ClinVar RCV Id: RCV001521649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Ala522Gly
CA8355410
NM_018081.2:c.1565C>G
CA2499224983
NM_018081.2:c.1565_1566delinsGA