Canonical Allele Identifier: PA2825803382
Gene: SLC46A3 HGNC NCBI
ClinVar RCV:
RCV004461811
ClinVar Variation:
3164941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129391.1:p.Leu74Met
CA247682989
NM_001135919.2:c.220C>A