Canonical Allele Identifier: PA645476092
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 404107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002373.3:p.Thr113Ser
CA16614130
NM_002382.5:c.337A>T
CA390031851
NM_002382.5:c.338C>G