Allele Registry

Canonical Allele Identifier: PA297000

Gene: MYL3 HGNC NCBI

ClinVar RCV:

RCV000158962

RCV000800210

ClinVar Variation:

181449

HGVS (amino-acid)	Matching Registered Transcripts
NP_000249.1:p.Met173Lys	CA013996 NM_000258.3:c.518T>A