Canonical Allele Identifier: PA2827103711
Gene: MYLK HGNC NCBI

Linked Data

ClinVar Variation Id: 936761
ClinVar RCV Id: RCV001205625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308238.1:p.Val554Leu
CA354234081
NM_001321309.2:c.1660G>T
CA354234082
NM_001321309.2:c.1660G>C