Canonical Allele Identifier: PA226705
Gene: RS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98947
ClinVar RCV Id: RCV000085287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000321.1:p.Trp122Cys
CA226703
NM_000330.3:c.366G>C
CA412372226
NM_000330.3:c.366G>T