Canonical Allele Identifier: PA2826295379
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224962
ClinVar RCV Id: RCV000210625 RCV000509419 RCV000494204 RCV001267141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001207411.1:p.Arg333del
CA10576003
NM_001220482.2:c.998_1000del
CA391926946
NM_001220482.2:c.997A>T
CA391926953
NM_001220482.2:c.994A>T
CA391926960
NM_001220482.2:c.991A>T