Canonical Allele Identifier: PA2829350305
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 1482566
ClinVar RCV Id: RCV002002958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002373.3:p.Ser129Arg
CA390031646
NM_002382.5:c.387C>A
CA390031648
NM_002382.5:c.387C>G
CA390031669
NM_002382.5:c.385A>C