Canonical Allele Identifier: PA138536
Gene: MYLK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149109.1:p.Pro144Ala
CA138534
NM_033118.4:c.430C>G