Canonical Allele Identifier: PA916012212
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 632903
ClinVar RCV Id: RCV000780466 RCV002360898 RCV003594038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser949Leu
CA346761082
NM_001281494.2:c.2846C>T