Canonical Allele Identifier: PA2573088202
Gene: SLC30A9 HGNC NCBI
ClinVar Allele:
1323887
ClinVar RCV:
RCV001807817
ClinVar Variation:
1333130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006336.3:p.Met50Val
CA2902149
NM_006345.4:c.148A>G