Canonical Allele Identifier: PA2830290843
Gene: SNX1 HGNC NCBI
ClinVar RCV:
RCV004136235
ClinVar Variation:
2282889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683758.1:p.Pro206Thr
CA7607849
NM_148955.4:c.616C>A