Canonical Allele Identifier: PA117726
Gene: SLC7A9 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055085.1:p.Gly195Arg
CA117725
NM_014270.5:c.583G>A
CA405202749
NM_014270.5:c.583G>C