Canonical Allele Identifier: PA1139758213
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 947847
ClinVar RCV Id: RCV001218991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660088.1:p.Arg60Trp
CA390035992
NM_145113.3:c.178C>T