Canonical Allele Identifier: PA658747994
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495714
ClinVar RCV Id: RCV000586843 RCV001019847 RCV001203154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe1103Cys
CA346758575
NM_000179.3:c.3308T>G