Canonical Allele Identifier: PA2830267989
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 1719259
ClinVar RCV Id: RCV002302019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660087.1:p.Asn116Tyr
CA390031748
NM_145112.3:c.346A>T