Canonical Allele Identifier: PA2573093428
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312936
ClinVar RCV Id: RCV001774390 RCV004040254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Leu53Phe
CA287494898
NM_018081.2:c.159G>T
CA397856800
NM_018081.2:c.159G>C