Canonical Allele Identifier: PA2826636507
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455213
ClinVar RCV Id: RCV000529411 RCV000581939 RCV001000818 RCV003459169 RCV004003681 RCV004546513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys583Glu
CA346755166
NM_001281494.2:c.1747A>G