Canonical Allele Identifier: PA234960
Gene: SMC1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167705
ClinVar RCV Id: RCV000153975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268392.1:p.Ala590Thr
CA234957
NM_001281463.1:c.1768G>A