Canonical Allele Identifier: PA645378620
Gene: SMARCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430455
ClinVar RCV Id: RCV000494188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003061.3:p.Phe1204Leu
CA372788968
NM_003070.5:c.3610T>C
CA372788972
NM_003070.5:c.3612T>A
CA372788973
NM_003070.5:c.3612T>G