Canonical Allele Identifier: PA2741814968
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637975
ClinVar RCV Id: RCV003412577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Asp126Gly
CA412372168
NM_000330.3:c.377A>G