Canonical Allele Identifier: PA2826999367
Gene:

Linked Data

ClinVar Variation Id: 500788
ClinVar RCV Id: RCV000594426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305738.1:p.Pro267Ser
CA3639616
NM_001318809.2:c.799C>T