Canonical Allele Identifier: PA645420172
Gene: MLYCD HGNC NCBI

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Amino-acid Alleles

HGVS (amino-acid) Transcript change
NP_036345.2:p.Ser327Arg
NM_012213.3:c.979A>C

NM_012213.3:c.981T>A

NM_012213.3:c.981T>G