Canonical Allele Identifier: PA1139753839
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 991028
ClinVar RCV Id: RCV001279165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071415.1:p.Val129Ile
CA360010139
NM_022132.5:c.385G>A