Canonical Allele Identifier: PA340137
Gene: MLYCD HGNC NCBI

Linked Data

ClinVar Variation Id: 4059
ClinVar RCV Id: RCV000004274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036345.2:p.Gly3Asp
CA340136
NM_012213.3:c.8G>A