Canonical Allele Identifier: PA272878
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 161251
ClinVar RCV Id: RCV000148509 RCV001041963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Arg178Cys
CA272877
NM_001024382.2:c.532C>T