Canonical Allele Identifier: PA103775
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 449465
ClinVar RCV Id: RCV000522139 RCV001254080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Thr35Met
CA229593101
NM_000190.4:c.104C>T