Canonical Allele Identifier: PA2826630753
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2693765
ClinVar RCV Id: RCV003594731 RCV004364920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly297Glu
CA346749319
NM_001281493.2:c.890G>A