Canonical Allele Identifier: PA2573093431
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338422
ClinVar RCV Id: RCV001817793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Thr144Ser
CA397860086
NM_018081.2:c.430A>T
CA397860090
NM_018081.2:c.431C>G