Canonical Allele Identifier: PA180860
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177847
ClinVar RCV Id: RCV000475271 RCV000622129 RCV000766436 RCV001189962 RCV003314568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala868Pro
CA012698
NM_000257.4:c.2602G>C