Canonical Allele Identifier: PA108873
Gene: SRY HGNC NCBI
ClinVar RCV:
RCV000010398
ClinVar Variation:
9744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Ala113Thr
CA254871
NM_003140.3:c.337G>A