Canonical Allele Identifier: PA2826636309
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127572
ClinVar RCV Id: RCV000115392 RCV000195931 RCV000212667 RCV000412127 RCV001193702 RCV001354925 RCV003460814 RCV003997241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His535Gln
CA010333
NM_001281494.2:c.1605C>G
CA346754300
NM_001281494.2:c.1605C>A