Canonical Allele Identifier: PA109090
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 470196
ClinVar RCV Id: RCV000541250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Tyr127Cys
CA414941142
NM_003140.3:c.380A>G