ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA254877
Gene: SRY
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000010402
ClinVar Variation:
9748
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003131.1:p.Trp70Ter