Canonical Allele Identifier: PA2573167835
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1453716
ClinVar RCV Id: RCV002037970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Ala111Asp
CA412372352
NM_000330.3:c.332C>A