Canonical Allele Identifier: PA2825623676
Gene: SLC7A9 HGNC NCBI
ClinVar RCV:
RCV000949840
ClinVar Variation:
770656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119807.1:p.Ala214Thr
CA9358736
NM_001126335.2:c.640G>A