Canonical Allele Identifier: PA263769
Gene: SLC7A7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119578.1:p.Asn365Tyr
CA263766
NM_001126106.4:c.1093A>T