Canonical Allele Identifier: PA2827104747
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2098431
ClinVar RCV Id: RCV003030946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Asn1329Ser
CA071787
NM_001321309.2:c.3986A>G