Canonical Allele Identifier: PA916020850
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000006788
ClinVar Variation:
6419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro502Leu
CA340584
NM_001308122.2:c.1505C>T