Canonical Allele Identifier: PA2580322423
Gene: MYL9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2241405
ClinVar RCV Id: RCV004103364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006088.2:p.Lys170Asn
CA408799076
NM_006097.5:c.510A>C
CA408799079
NM_006097.5:c.510A>T