Canonical Allele Identifier: PA645439012
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 283448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Thr27Met
CA8643689
NM_000023.3:c.80C>T