Canonical Allele Identifier: PA658801226
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 487586
ClinVar RCV Id: RCV000656148 RCV001176897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Asn1973Ser
CA394843490
NM_001040114.2:c.5918A>G