Canonical Allele Identifier: PA658745033
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 492908
ClinVar RCV Id: RCV000581278
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Arg30Ile
CA414941829
NM_003140.3:c.89G>T