Canonical Allele Identifier: PA2573187948
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1486120
ClinVar RCV Id: RCV002001246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245137.1:p.Val215Leu
CA382896825
NM_001258208.2:c.643G>C
CA382896829
NM_001258208.2:c.643G>T