Canonical Allele Identifier: PA177176
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 164491
ClinVar RCV Id: RCV000151371 RCV000530942 RCV000621707 RCV000777989 RCV000625226 RCV001576618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Ala2Pro
CA013963
NM_000258.3:c.4G>C