Canonical Allele Identifier: PA2830142964
Gene: MYLK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444259.1:p.Val138Met
CA354228503
NM_053031.4:c.412G>A