Canonical Allele Identifier: PA2829384955
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3212877
ClinVar RCV Id: RCV004503797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Leu257Val
CA356138818
NM_002448.3:c.769C>G