Canonical Allele Identifier: PA092857
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9892
ClinVar RCV Id: RCV000010570 RCV000085290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Leu13Pro
CA226709
NM_000330.3:c.38T>C