Canonical Allele Identifier: PA916056538
Gene: B9D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 684427
ClinVar RCV Id: RCV000993853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085055.2:p.His5Gln
CA406012138
NM_030578.4:c.15C>G
CA406012139
NM_030578.4:c.15C>A