Allele Registry

Canonical Allele Identifier: PA340139

Gene: MLYCD HGNC NCBI

ClinVar RCV:

RCV000004275

ClinVar Variation:

4060

HGVS (amino-acid)	Matching Registered Transcripts
NP_036345.2:p.Met40Thr	CA340138 NM_012213.3:c.119T>C