Canonical Allele Identifier: PA149062
Gene: MCCC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 95941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064551.3:p.His464Pro
CA149061
NM_020166.5:c.1391A>C