Canonical Allele Identifier: PA2826314486
Gene: SLC7A9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229965.1:p.Ala214Thr
CA9358736
NM_001243036.2:c.640G>A