Canonical Allele Identifier: PA915958256
Gene: SAPCD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403113
ClinVar RCV Id: RCV000455422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034740.1:p.Pro99Leu
CA3721746
NM_001039651.2:c.296C>T