Canonical Allele Identifier: PA2826635917
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525835
ClinVar RCV Id: RCV000630178 RCV002420672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe444Leu
CA346752552
NM_001281494.2:c.1330T>C
CA346752567
NM_001281494.2:c.1332T>A
CA346752570
NM_001281494.2:c.1332T>G