Canonical Allele Identifier: PA645376306
Gene: B9D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 254680
ClinVar RCV Id: RCV000241542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056496.1:p.Val174del
CA10586696
NM_015681.6:c.520_522del