Canonical Allele Identifier: PA2826313288
Gene: SNX1 HGNC NCBI
ClinVar RCV:
RCV004136235
ClinVar Variation:
2282889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Pro271Thr
CA7607849
NM_001242933.2:c.811C>A