Canonical Allele Identifier: PA253034
Gene: SMARCAL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Arg586Trp
CA253032
NM_014140.4:c.1756C>T