Canonical Allele Identifier: PA092732
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98956
ClinVar RCV Id: RCV000085297 RCV001003218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Gly140Arg
CA226722
NM_000330.3:c.418G>A
CA412371884
NM_000330.3:c.418G>C