Canonical Allele Identifier: PA146062
Gene: MID1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92878
ClinVar RCV Id: RCV000078680 RCV000659859 RCV000950878 RCV002311555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_150632.1:p.Pro667Leu
CA146060
NM_033290.4:c.2000C>T