Canonical Allele Identifier: PA2741862562
Gene: SAP25 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335606.1:p.Arg91Trp
CA163273628
NM_001348677.2:c.271C>T