Canonical Allele Identifier: PA645503097
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 421320
ClinVar RCV Id: RCV000485988 RCV000546123 RCV000565111 RCV002481518 RCV003470569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn1719Ser
CA6265636
NM_000051.4:c.5156A>G