Canonical Allele Identifier: PA2573227938
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 1490028
ClinVar RCV Id: RCV002001650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Arg76Cys
CA414941508
NM_003140.3:c.226C>T