Canonical Allele Identifier: PA2828100894
Gene: MSX2 HGNC NCBI
ClinVar RCV:
RCV003871639
ClinVar Variation:
3019008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350555.1:p.Ala72Gly
CA362229356
NM_001363626.2:c.215C>G