Canonical Allele Identifier: PA1139696645
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 948950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307344.1:p.Ser78Thr
CA390031425
NM_001320415.2:c.233G>C