Canonical Allele Identifier: PA288232
Gene: HOXB13 HGNC NCBI

Linked Data

ClinVar Variation Id: 128033
ClinVar RCV Id: RCV000115971 RCV000567230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Val146Met
CA288230
NM_006361.6:c.436G>A