Canonical Allele Identifier: PA2573258155
Gene: SMARCAL1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054859.2:p.Ala20Gly
CA350496286
NM_014140.4:c.59C>G