Canonical Allele Identifier: PA2573167831
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1453240
ClinVar RCV Id: RCV001994760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Ala111Val
CA412372350
NM_000330.3:c.332C>T