Canonical Allele Identifier: PA2826631097
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773645
ClinVar RCV Id: RCV003584501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys374Asn
CA346750715
NM_001281493.2:c.1122A>C
CA346750716
NM_001281493.2:c.1122A>T