Canonical Allele Identifier: PA2741918795
Gene: OMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2558778
ClinVar RCV Id: RCV004325601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005005.1:p.Ser201Phe
CA5124513
NM_005014.3:c.602C>T