Canonical Allele Identifier: PA109060
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 9754
ClinVar RCV Id: RCV000010408
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Ser18Asn
CA254886
NM_003140.3:c.53G>A