Canonical Allele Identifier: PA2826633388
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141188
ClinVar RCV Id: RCV000129582 RCV000411815 RCV000479516 RCV000780465 RCV000810760 RCV003460896 RCV003997512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met900Val
CA013509
NM_001281493.2:c.2698A>G