Canonical Allele Identifier: PA2825333172
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 851793
ClinVar RCV Id: RCV001056264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Met195Ile
CA382896764
NM_001024382.2:c.585G>A
CA382896766
NM_001024382.2:c.585G>T
CA382896770
NM_001024382.2:c.585G>C