Canonical Allele Identifier: PA2826631652
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127570
ClinVar RCV Id: RCV000115390 RCV000199520 RCV000409470 RCV000491756 RCV000656895 RCV000708875 RCV000765687 RCV001249960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu505Lys
CA010227
NM_001281493.2:c.1513G>A