Canonical Allele Identifier: PA2741814916
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2785684
ClinVar RCV Id: RCV003664518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Leu13Val
CA412379051
NM_000330.3:c.37C>G