Canonical Allele Identifier: PA2573062050
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331924
ClinVar RCV Id: RCV001804440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1294Asn
CA389041719
NM_000257.4:c.3882G>T
CA389041720
NM_000257.4:c.3882G>C