Canonical Allele Identifier: PA2827044839
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 1714657
ClinVar RCV Id: RCV002299038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307344.1:p.Asp56Gly
CA390031802
NM_001320415.2:c.167A>G