Canonical Allele Identifier: PA1139696613
Gene: MAX HGNC NCBI

Linked Data

ClinVar Variation Id: 841737
ClinVar RCV Id: RCV001044019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307344.1:p.Ala63Ser
CA390031728
NM_001320415.2:c.187G>T