Canonical Allele Identifier: PA2829350287
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 1719259
ClinVar RCV Id: RCV002302019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002373.3:p.Asn125Tyr
CA390031748
NM_002382.5:c.373A>T