Allele Registry

Canonical Allele Identifier: PA132611

Gene: MYL2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000024457

RCV000148715

RCV000157368

RCV000234981

RCV000254541

RCV000528536

RCV000584767

RCV000769367

RCV002504822

RCV003996116

ClinVar Variation:

31766

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000423.2:p.Asn47Lys	CA009871 NM_000432.4:c.141C>A CA386699300 NM_000432.4:c.141C>G