Canonical Allele Identifier: PA2826635897
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1787961
ClinVar RCV Id: RCV002428106
ClinVar Variation Id: 2743826
ClinVar RCV Id: RCV003593561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn439Lys
CA346752447
NM_001281494.2:c.1317C>A
CA346752450
NM_001281494.2:c.1317C>G