Canonical Allele Identifier: PA916024512
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 662389
ClinVar RCV Id: RCV000820017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307344.1:p.Pro53Ala
CA390031831
NM_001320415.2:c.157C>G