Canonical Allele Identifier: PA234961
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167705
ClinVar RCV Id: RCV000153975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006297.2:p.Ala612Thr
CA234957
NM_006306.4:c.1834G>A