Canonical Allele Identifier: PA2828079999
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1524591
ClinVar RCV Id: RCV002031833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350076.1:p.Gly233Arg
CA359986078
NM_001363147.1:c.697G>A
CA359986081
NM_001363147.1:c.697G>C