Canonical Allele Identifier: PA2830171433
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1935496
ClinVar RCV Id: RCV002639023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_570711.2:p.Thr438Ser
CA381180206
NM_130799.3:c.1313C>G
CA381180209
NM_130799.3:c.1312A>T