Canonical Allele Identifier: PA2826630747
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428400
ClinVar RCV Id: RCV000491701 RCV001865527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu295Asp
CA346749291
NM_001281493.2:c.885A>C
CA346749293
NM_001281493.2:c.885A>T