Canonical Allele Identifier: PA2830170658
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 36529
ClinVar RCV Id: RCV000030202
ClinVar Variation Id: 1677022
ClinVar RCV Id: RCV002222880 RCV003517356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.His139Gln
CA009417
NM_130799.3:c.417C>G
CA381186782
NM_130799.3:c.417C>A