Canonical Allele Identifier: PA2826930003
Gene: SS18 HGNC NCBI

Linked Data

ClinVar Variation Id: 2531249
ClinVar RCV Id: RCV004299619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295130.1:p.Pro260Ser
CA402079884
NM_001308201.2:c.778C>T