Canonical Allele Identifier: PA2826000167
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 345316
ClinVar RCV Id: RCV000286229 RCV003969995 RCV001573460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Gly222Arg
CA2230505
NM_001164675.2:c.664G>C
CA351632643
NM_001164675.2:c.664G>A