Canonical Allele Identifier: PA2826765387
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_001276325.1:p.Phe1204Leu
CA372788968
NM_001289396.1:c.3610T>C
CA372788972
NM_001289396.1:c.3612T>A
CA372788973
NM_001289396.1:c.3612T>G