Canonical Allele Identifier: PA2826631307
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127568
ClinVar RCV Id: RCV000115387 RCV000219041 RCV000630209 RCV003997240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala422Gly
CA009795
NM_001281493.2:c.1265C>G