Canonical Allele Identifier: PA2830268000
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 1482566
ClinVar RCV Id: RCV002002958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660087.1:p.Ser120Arg
CA390031646
NM_145112.3:c.360C>A
CA390031648
NM_145112.3:c.360C>G
CA390031669
NM_145112.3:c.358A>C