Canonical Allele Identifier: PA2826631521
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495707
ClinVar RCV Id: RCV000587268 RCV000772486 RCV000821395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln474His
CA346753318
NM_001281493.2:c.1422A>C
CA346753321
NM_001281493.2:c.1422A>T