Canonical Allele Identifier: PA2828403206
Gene: MEN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1935496
ClinVar RCV Id: RCV002639023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357192.2:p.Thr403Ser
CA381180206
NM_001370263.2:c.1208C>G
CA381180209
NM_001370263.2:c.1207A>T