Canonical Allele Identifier: PA916011462
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 221123
ClinVar RCV Id: RCV000205915 RCV000216977 RCV000486074 RCV000764432 RCV003155125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe974Leu
CA070636
NM_001281492.2:c.2922T>A
CA346758586
NM_001281492.2:c.2920T>C
CA346758604
NM_001281492.2:c.2922T>G