Canonical Allele Identifier: PA658677542
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 461600
ClinVar RCV Id: RCV000560292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Gly122Val
CA2832952
NM_002448.3:c.365G>T