Canonical Allele Identifier: PA2580450184
Gene: MCCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2336913
ClinVar RCV Id: RCV002931105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071415.1:p.Ser328Arg
CA359987797
NM_022132.5:c.982A>C
CA359987808
NM_022132.5:c.984C>A
CA359987810
NM_022132.5:c.984C>G