Canonical Allele Identifier: PA198942
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43100
ClinVar RCV Id: RCV000035995 RCV000622036 RCV000762926 RCV000162339 RCV000628940 RCV001170745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp239Asn
CA016679
NM_000257.4:c.715G>A