Canonical Allele Identifier: PA2580491038
Gene: SLC38A5 HGNC NCBI
ClinVar Allele:
2342148
ClinVar RCV:
RCV004191739
ClinVar Variation:
2349764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277053.2:p.Val296Met
CA10402249
NM_033518.3:c.886G>A