Canonical Allele Identifier: PA2741912037
Gene: BST1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2511247
ClinVar RCV Id: RCV004282333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004325.2:p.Pro167Ala
CA2865400
NM_004334.3:c.499C>G