Canonical Allele Identifier: PA2827105173
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002345055
ClinVar Variation:
1748726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Asp1701Tyr
CA354228835
NM_001321309.2:c.5101G>T