Canonical Allele Identifier: PA2830141526
Gene: MYLK HGNC NCBI
ClinVar RCV:
RCV002345055
ClinVar Variation:
1748726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Asp1826Tyr
CA354228835
NM_053027.4:c.5476G>T