Canonical Allele Identifier: PA913191588
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 631350
ClinVar RCV Id: RCV000777538 RCV003605691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr915Ser
CA382545405
NM_000051.4:c.2743A>T
CA382545409
NM_000051.4:c.2744C>G