Canonical Allele Identifier: PA916010928
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232956
ClinVar RCV Id: RCV000216301 RCV000479204 RCV000814244 RCV003998016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn21Lys
CA10578021
NM_001281492.2:c.63C>G
CA346734573
NM_001281492.2:c.63C>A