Canonical Allele Identifier: PA2830267956
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 662389
ClinVar RCV Id: RCV000820017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660087.1:p.Pro107Ala
CA390031831
NM_145112.3:c.319C>G