Canonical Allele Identifier: PA2580414315
Gene: SIX2 HGNC NCBI
ClinVar RCV:
RCV002909510
ClinVar Variation:
2049063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_058628.3:p.Val255Ala
CA1642475
NM_016932.5:c.764T>C