Canonical Allele Identifier: PA092931
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 9895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Pro203Leu
CA226813
NM_000330.3:c.608C>T