Canonical Allele Identifier: PA915989448
Gene: SNX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 719339
ClinVar RCV Id: RCV000892458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057060.2:p.Phe250Leu
CA964085
NM_015976.5:c.750C>A
CA341381973
NM_015976.5:c.748T>C
CA341381978
NM_015976.5:c.750C>G