Canonical Allele Identifier: PA108996
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 9747
ClinVar RCV Id: RCV000010401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003131.1:p.Met64Ile
CA254875
NM_003140.3:c.192G>A
CA414941586
NM_003140.3:c.192G>T
CA414941587
NM_003140.3:c.192G>C