Canonical Allele Identifier: PA2829561385
Gene: SCAF11 HGNC NCBI
ClinVar RCV:
RCV004452529
ClinVar Variation:
3158139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004710.2:p.Met744Lys
CA236405414
NM_004719.3:c.2231T>A