Canonical Allele Identifier: PA102630
Gene: SLC7A9 HGNC NCBI
ClinVar RCV:
RCV000006136
ClinVar Variation:
5780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119807.1:p.Val170Met
CA117721
NM_001126335.2:c.508G>A