Canonical Allele Identifier: PA916024508
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 404107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307344.1:p.Thr50Ser
CA16614130
NM_001320415.2:c.148A>T
CA390031851
NM_001320415.2:c.149C>G