Canonical Allele Identifier: PA2830268055
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 2587741
ClinVar RCV Id: RCV003360973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660087.1:p.Ser142Arg
CA390031225
NM_145112.3:c.426C>A
CA390031227
NM_145112.3:c.426C>G
CA390031242
NM_145112.3:c.424A>C