Canonical Allele Identifier: PA916020754
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000625694
ClinVar Variation:
522551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Met229Arg
CA360804849
NM_001308122.2:c.686T>G