Allele Registry

Canonical Allele Identifier: PA101477

Gene: SLC7A7 HGNC NCBI

ClinVar RCV:

RCV000049762

ClinVar Variation:

56349

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119577.1:p.Asn365Tyr	CA263766 NM_001126105.3:c.1093A>T