Canonical Allele Identifier: PA092720
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98952
ClinVar RCV Id: RCV000085293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Gly135Val
CA226715
NM_000330.3:c.404G>T