Canonical Allele Identifier: PA108974
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 9742
ClinVar RCV Id: RCV000010396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Lys106Ile
CA254869
NM_003140.3:c.317A>T