Canonical Allele Identifier: PA2580471619
Gene: B9D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2268607
ClinVar RCV Id: RCV004125357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085055.2:p.Ala2Thr
CA406012179
NM_030578.4:c.4G>A