Canonical Allele Identifier: PA2580498214
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1977010
ClinVar RCV Id: RCV002736423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_444255.3:p.Trp722Gly
CA354234132
NM_053027.4:c.2164T>G