Canonical Allele Identifier: PA210354
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 191728
ClinVar RCV Id: RCV000172044 RCV000201892 RCV000290332 RCV000345240 RCV000384692 RCV000313875 RCV000390901 RCV000777701 RCV001823718 RCV003320133 RCV002478549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1441Ser
CA014807
NM_000257.4:c.4321G>T