Canonical Allele Identifier: PA138524
Gene: MYLK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 46522
ClinVar RCV Id: RCV000039784 RCV000172570 RCV000770567 RCV001081175 RCV001293152
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149109.1:p.Ala58Asp
CA138522
NM_033118.4:c.173C>A