Canonical Allele Identifier: PA109016
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 9738
ClinVar RCV Id: RCV000010391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Phe109Ser
CA254865
NM_003140.3:c.326T>C