Canonical Allele Identifier: PA1139750128
Gene: HOXA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 911504
ClinVar RCV Id: RCV001163996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705873.3:p.Ser98Arg
CA4195967
NM_153620.3:c.294C>G
CA367068923
NM_153620.3:c.294C>A
CA367068931
NM_153620.3:c.292A>C