Canonical Allele Identifier: PA2826454767
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1953004
ClinVar RCV Id: RCV002672149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245137.1:p.Ala112Gly
CA382891114
NM_001258208.2:c.335C>G