Canonical Allele Identifier: PA2580271789
Gene: MSX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161115
ClinVar RCV Id: RCV003078414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002439.2:p.Met146Ile
CA2832971
NM_002448.3:c.438G>A
CA2832972
NM_002448.3:c.438G>T
CA356138110
NM_002448.3:c.438G>C