Canonical Allele Identifier: PA2573227937
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 1470948
ClinVar RCV Id: RCV001964433
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Ser71Tyr
CA414941541
NM_003140.3:c.212C>A